510(k) K991980 ยท KNW Instrument, Biopsy
MAMMOTOME HH HAND-HELD PROBE, VACUUM SET, CONTROL MODULE, HH HAND-HELD HOLSTER AND CABLES, SOFTWARE PACKAGE, FOOTSWITCH,
| Applicant | Ethicon Endo-Surgery, Inc., Cincinnati OH, US |
| Decision | Substantially Equivalent, Aug 17, 1999 |
| Received | Jun 14, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991980
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.