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Code Of Federal Regulations Title 21, Volume 8, April 1, 2015 [Paperback]

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  • Category: Books (Law)
  • ISBN-10:  1354240235
  • ISBN-10:  1354240235
  • ISBN-13:  9781354240236
  • ISBN-13:  9781354240236
  • Publisher:  Regulations Press
  • Publisher:  Regulations Press
  • Pages:  862
  • Pages:  862
  • Binding:  Paperback
  • Binding:  Paperback
  • Pub Date:  01-Jun-2016
  • Pub Date:  01-Jun-2016
  • SKU:  1354240235-11-MPOD
  • SKU:  1354240235-11-MPOD
  • Item ID: 100740415
  • Seller: ShopSpell
  • Ships in: 2 business days
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  • Delivery by: Apr 08 to Apr 10
  • Notes: Brand New Book. Order Now.
21 CFR Parts 800 to 1299 covers the U. S. Food and Drug Administration within the U.S. Department of Health and Human Services. Within this volume, you will find rules, procedures, and regulations pertaining to medical devices, such as cardiovascular devices, dentistry devices, orthopedic, gastroenterology-urology, in vitro, anesthesiology, and more. Plus, you will find rules, procedures, and regulations relating to mammography quality standards, radiological health, tobacco products, human tissue intended for transplantation, and more.Health care device manufacturers, hospital radiological and other medical technicians and departments, physicians, nurses, out-patient clinics' personnel, and health care policy advocates may be interested in this volume.Code of Federal Regulations Title 21, Volume 8, April 1, 2015Containing parts Parts 800 to 1299Part 800; GENERALPart 801; LABELINGPart 803; MEDICAL DEVICE REPORTING; (Eff. Until 8-14-15)Part 806; MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALSPart 807; ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICESPart 808; EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTSPart 809; IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USEPart 810; MEDICAL DEVICE RECALL AUTHORITYPart 812; INVESTIGATIONAL DEVICE EXEMPTIONSPart 813; ReservedPart 814; PREMARKET APPROVAL OF MEDICAL DEVICESPart 820; QUALITY SYSTEM REGULATIONPart 821; MEDICAL DEVICE TRACKING REQUIREMENTSPart 822; POSTMARKET SURVEILLANCEPart 830; UNIQUE DEVICE IDENTIFICATIONPart 860; MEDICAL DEVICE CLASSIFICATION PROCEDURESPart 861; PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENTPart 862; CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICESPart 864; HEMATOLOGY AND PATHOLOGY DEVICESPart 866; IMMUNOLOGY AND MICROBIOLOGY DEVICESPart 868; ANESTHESIOLOGY DEVICESPart 870; CARDIOVASCULAR DEVICESPart 872; DENTAL DEVICESPart 874; EAR, NOSE, AND THROAT DEVICESPart 876; GASTROENTEROLOGY-UROLOGY DEVICESPart 878; GENERl“.
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