FDA-CYBERSECURITY-MA › Postmarket Management of Cybersecurity in Medical Devices
Postmarket Management of Cybersecurity in Medical Devices
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:
IEC-60601-1Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
UL-913
Standard for Intrinsically Safe Apparatus and Associated Apparatus for Use in Class I, II, III, Division 1, Hazardous (Classified) Locations
ASTM-F1980
Standard Guide for Accelerated Aging of Sterile Barrier Systems and Medical Devices
Document Number
FDA-CYBERSECURITY-MA
Revision Level
2016 EDITION
Status
Current
Publication Date
Dec. 28, 2016
Page Count
30 pages