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631	NOV Exhibit S 510(k) Summary Date of Summary Preparation: January IS. 2013 Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-09 11:45:15 Radiography Projectional radiography Digital radiography Medical imaging X-ray Title 21 of the Code of Federal Regulations Medical device Food and Drug Administration Medicine Medical physics Radiology
632	Section[removed]k) Summary 1 Manufacturing Establishment and Contact Information Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-05-28 00:34:50 Food law Radiography Fluoroscopy X-ray image intensifier Federal Food Drug and Cosmetic Act Hologic Premarket approval Medical device Title 21 of the Code of Federal Regulations Medicine Health Food and Drug Administration
633	NOV[removed]k) Submission- RAYSCAN a-Expert Special 510(k) Summary The summary of 510(k) safety and effectiveness information is being submitted in accordance with the requirements of 21 CFR Part[removed]. Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-09 11:45:28 Dental radiography Medical device X-ray Title 21 of the Code of Federal Regulations Center for Devices and Radiological Health Medicine Projectional radiography Orthopantomogram
634	~DL IRA ~Section IIEi~ K(o3IR 7 Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-04-25 00:30:43 Health Food law Medical technology Medical equipment Medical device Federal Food Drug and Cosmetic Act X-ray computed tomography Premarket approval Title 21 of the Code of Federal Regulations Medicine Technology Food and Drug Administration
635	Federal Register / Vol. 66, No[removed]Friday, February 23, [removed]Rules and Regulations (x) Chief; Decennial Statistical Studies Division; (xi) Chief; Population Division; and (xii) Senior Mathematical Statistician. § 10 Add to Reading List Source URL: www.epa.gov Language: English - Date: 2001-05-07 16:07:43 Law Regulatory Flexibility Act United States Environmental Protection Agency Federal Register Title 21 CFR Part 11 Code of Federal Regulations United States administrative law Government Politics of the United States
636	JAN[removed]k) Submission - 1417YPCA 510(k) Summary This summary of 510(k) safety and effectiveness information is being submitted in accordance with Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-02-11 08:44:11 Radiography Medical physics Food law Center for Devices and Radiological Health Title 21 of the Code of Federal Regulations Medical device X-ray Premarket approval Federal Food Drug and Cosmetic Act Medicine Medical imaging Food and Drug Administration
637	NEPK Electron Co PO. Box 12, Saint-Petersburg, Russia[removed]ELECTRONTel. +7 Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-11-09 20:54:05 Radiography Food law Medical imaging Medical device Premarket approval Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Center for Devices and Radiological Health X-ray Medicine Food and Drug Administration Medical physics
638	3D Imaging & Simulations Corp. 510(k) Summary for K131442 This summary of 510(k) safety and effectiveness information is being submitted in accordance with requirements of 21 CFR Part[removed]Date Prepared: September 3. Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-10-09 09:32:45 Medical physics Telehealth Projectional radiography Digital radiography Computed radiography DICOM X-ray Radiology Picture archiving and communication system Medicine Medical imaging Radiography
639	510(k) Summary K121345 Halifax Biomedical Inc[removed]Route 1%, Mabou Nova Scotia, Canada, BOE 1X0 Phone +[removed] Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-07-06 14:45:24 Food law Medical physics Projectional radiography Medical device X-ray Federal Food Drug and Cosmetic Act Premarket approval Digital radiography Title 21 of the Code of Federal Regulations Medicine Medical imaging Food and Drug Administration
640	510(k) Submission - PaX-i Special 510(k) Summary SEP Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-10-09 13:29:34 Food law Digital radiography Medical technology Medical device Premarket approval X-ray Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Dental radiography Medicine Projectional radiography Food and Drug Administration

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