510(k) K030472 ยท KNW Instrument, Biopsy
MAMMOTOME BIOPSY SYSTEM PROBE & HOUSING, MAMMOTOME HAND-HELD SYSTEM
| Applicant | Ethicon Endo-Surgery, Inc., Cincinnati OH, US |
| Decision | Substantially Equivalent, Oct 9, 2003 |
| Received | Feb 12, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030472
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.