510(k) K981721 ยท KNW Instrument, Biopsy
C0-AXIAL INTRODUCER NEEDLE
| Applicant | Inrad, Kentwood MI, US |
| Decision | Substantially Equivalent, Jul 28, 1998 |
| Received | May 15, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981721
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.