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

nlm:nlmuid-101713256-pdf

6. Medical product communications that are consistent with the FDA-required labeling: questions and answers

nlm:nlmuid-101734292-pdf

7. Appropriate use of voluntary consensus standards in premarket submissions for medical devices: guidance for industry and Food and Drug Administration staff

nlm:nlmuid-101734447-pdf

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

nlm:nlmuid-101719889-pdf

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

nlm:nlmuid-101719980-pdf

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

nlm:nlmuid-101720008-pdf