510(k) K883374 ยท KNW Instrument, Biopsy
BARD BIOPSY NEEDLE GUIDANCE DEVICE
| Applicant | C.R. Bard, Inc., Billerica MA, US |
| Decision | Substantially Equivalent, Sep 29, 1988 |
| Received | Aug 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883374
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.