510(k) K023923 ยท KNW Instrument, Biopsy
SENOCOR 360 CIRCUMFERENTIAL VACUUM ASSISTED BIOPSY DEVICE, 8 GAUGE
| Applicant | Senorx, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Dec 11, 2002 |
| Received | Nov 25, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023923
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.