510(k) K980676 ยท KNW Instrument, Biopsy
SPIGAL NEEDLE
| Applicant | Gallini U.S., LLC, Richmond VA, US |
| Decision | Substantially Equivalent, May 21, 1998 |
| Received | Feb 20, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980676
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.