510(k) K034021 ยท KNW Instrument, Biopsy
VACUUM ASSISTED CORE BIOPSY DEVICE
| Applicant | Suros Surgical Systems, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Sep 8, 2004 |
| Received | Dec 24, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K034021
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.