510(k) K934371 ยท KNW Instrument, Biopsy
BIP MULTI MODIFICATION
| Applicant | Bip USA, Inc., Niagara Falls NY, US |
| Decision | Substantially Equivalent, Apr 28, 1994 |
| Received | Sep 7, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934371
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.