510(k) K042136 ยท KNW Instrument, Biopsy
SANARUS CASSI ROTATIONAL CORE BIOPSY SYSTEM
| Applicant | Sanarus Medical, Inc., Pleasanton CA, US |
| Decision | Substantially Equivalent, Sep 8, 2004 |
| Received | Aug 9, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K042136
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.