510(k) K033700 ยท KNW Instrument, Biopsy
MAMMOTOME EX HAND HELD SYSTEM
| Applicant | Ethicon Endo-Surgery, Inc., Cincinnati OH, US |
| Decision | Substantially Equivalent, Feb 20, 2004 |
| Received | Nov 25, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033700
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 27, 2005 | Ethicon Endo-Surgery Mammotome EX Holster Terminated |
KNW | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.