510(k) K873369 ยท KNW Instrument, Biopsy
SECURLINE FRANSEENE NEEDLE
| Applicant | Precision Dynamics Corp., Van Nuys CA, US |
| Decision | Substantially Equivalent, Oct 20, 1987 |
| Received | Aug 21, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873369
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.