510(k) K981796 ยท KNW Instrument, Biopsy
LIGHT SABER CORE TISSUE NEEDLE
| Applicant | Minrad, Inc., Orchard Park NY, US |
| Decision | Substantially Equivalent, Aug 5, 1998 |
| Received | May 21, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981796
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.