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1. Manufacturers sharing patient-specific information from medical devices with patients upon request: guidance for industry and Food and Drug Administration staff

2. Unique device identification: direct marking of devices : guidance for Industry and Food and Drug administration staff

3. Software as a medical device (SAMD): clinical evaluation : guidance for industry and Food and Drug Administration staff

4. FDA should further integrate its review of cybersecurity into the premarket review process for medical devices

6. Design considerations and pre-market submission recommendations for interoperable medical devices: guidance for industry and Food and Drug Administration staff

8. Medical devices containing materials derived from animal sources (except for in vitro diagnostic devices): guidance for industry and Food and Drug Administration staff

9. Recommended content and format of non-clinical bench performance testing information in premarket submissions: guidance for industry and Food and Drug Administration staff

10. 30-Day notices, 135-day premarket approval (PMA) supplements and 75-day humanitarian device exemption (HDE) supplements for manufacturing method or process changes: guidance for industry and Food and Drug Administration staff