510(k) K011104 ยท KNW Instrument, Biopsy
OSTEOBELL
| Applicant | Biopsybell S.A.S., South Glastonbury CT, US |
| Decision | Substantially Equivalent, May 31, 2001 |
| Received | Apr 11, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011104
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.