FDA-WELLNESS › General Wellness: Policy for Low Risk Devices - Guidance for Industry and Food and Drug Administration Staff
General Wellness: Policy for Low Risk Devices - Guidance for Industry and Food and Drug Administration Staff
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:
BS-EN-ISO/IEC-17025General requirements for the competence of testing and calibration laboratories
29CFR(1900-1910.999)-PDF
Labor - PDF Format
BS-EN-ISO-14155
Clinical investigation of medical devices for human subjects. Good clinical practice
Document Number
1300013
Revision Level
2019 EDITION
Status
Current
Publication Date
Sept. 27, 2019
Page Count
12 pages