510(k) K951229 ยท KNW Instrument, Biopsy
MODIFIED BIOPSY NEEDLE
| Applicant | Biopsys Medical, Inc., San Juan Capistrano CA, US |
| Decision | Substantially Equivalent, Apr 6, 1995 |
| Received | Mar 20, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951229
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.