510(k) K861267 ยท KNW Instrument, Biopsy
UROCUT BIOPSY NEEDLE
| Applicant | Meadox Surgimed, Inc., Oakland NJ, US |
| Decision | Substantially Equivalent, Jan 20, 1987 |
| Received | Apr 4, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861267
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.