510(k) K010735 ยท KNW Instrument, Biopsy
SPEEDYBELL
| Applicant | Biopsybell S.A.S., South Glastonbury CT, US |
| Decision | Substantially Equivalent, Aug 17, 2001 |
| Received | Mar 12, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010735
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.