FDA-INTERACTIVE REVI Types of Communication During the Review of Medical Device Submissions - Guidance for Industry and Food and Drug Administration Staff (Originally titled: Interactive Review for Medical Device Submissions: 510(k)s, Original PMAs, PMA Supplements, Original BLAs, and BLA Supplements)

FDA-INTERACTIVE REVI - 2014 EDITION - CURRENT
Show Complete Document History


Types of Communication During the Review of Medical Device Submissions - Guidance for Industry and Food and Drug Administration Staff (Originally titled: Interactive Review for Medical Device Submissions: 510(k)s, Original PMAs, PMA Supplements, Original BLAs, and BLA Supplements)


This document comes with our free Notification Service, good for the life of the document.

This document is available in either Paper or PDF format.

 

Customers who bought this document also bought:

SOR/98-282
Medical Devices Regulations (Canada)

BS-EN-ISO-13485
Medical devices. Quality management systems. Requirements for regulatory purposes

BS-EN-ISO-15223-1
Medical devices. Symbols to be used with information to be supplied by the manufacturer

ORDER

Price:

$20.00        




Document Number

FDA-INTERACTIVE REVI

Revision Level

2014 EDITION

Status

Current

Publication Date

April 2, 2014

Page Count

15 pages