Postmarketing surveillance of medical devices--filling in the gaps

N Engl J Med. 2012 Mar 8;366(10):875-7. doi: 10.1056/NEJMp1114865. Epub 2012 Feb 14.
No abstract available

MeSH terms

  • Databases, Factual
  • Device Approval
  • Equipment Failure*
  • Humans
  • Patient Safety
  • Product Surveillance, Postmarketing* / methods
  • Registries*
  • United States
  • United States Food and Drug Administration