510(k) K963813 ยท KNW Instrument, Biopsy
SURE CORE BIOPSY KIT
| Applicant | Interventional Concepts, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Mar 20, 1997 |
| Received | Sep 23, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963813
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.