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2. Registration and product listing for owners and operators of domestic tobacco product establishments: (revised)

nlm:nlmuid-101733965-pdf

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

nlm:nlmuid-101734292-pdf

6. Display devices for diagnostic radiology: guidance for industry and Food and Drug Administration staff

nlm:nlmuid-101719840-pdf

7. Deciding when to submit a 510(k) for a change to an existing device: guidance for Industry and Food and Drug Administration staff

nlm:nlmuid-101719884-pdf

8. Product labeling for certain ultrasonic surgical aspirator devices: guidance for Industry and Food and Drug Administration staff

nlm:nlmuid-101719888-pdf

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

nlm:nlmuid-101719980-pdf

10. Pediatric information for x-ray imaging device premarket notifications: guidance for industry and Food and Drug Administration staff

nlm:nlmuid-101719987-pdf