510(k) K973215 ยท KNW Instrument, Biopsy
STEREOTACTIC NEEDLE CORE BIOPSY SYSTEM
| Applicant | Laurus Medical Corp., Irvine CA, US |
| Decision | Substantially Equivalent, Nov 6, 1997 |
| Received | Aug 27, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973215
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.