510(k) K891777 ยท FCG Biopsy Needle
PRO-CUT BIOPSY NEEDLE
| Applicant | Teknar, Inc., Fenton MO, US |
| Decision | Substantially Equivalent, May 4, 1989 |
| Received | Mar 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891777
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.