510(k) K924106 ยท KNW Instrument, Biopsy
BIOPSY FORCEPS
| Applicant | United States Endoscopy Group, Inc., Mentor OH, US |
| Decision | Substantially Equivalent, Nov 24, 1992 |
| Received | Aug 13, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924106
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.