510(k) K032506 ยท KNW Instrument, Biopsy
SANARUS CENTRICA II ROTATIONAL CORE BIOPSY SYSTEM
| Applicant | Sanarus Medical, Inc., Pleasanton CA, US |
| Decision | Substantially Equivalent, Oct 9, 2003 |
| Received | Aug 14, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032506
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.