510(k) K872597 ยท DWO Needle, Biopsy, Cardiovascular
FINE NEEDLE ASPIRATION BIOPSY SYSTEM-PROSTATE
| Applicant | Dianon Systems, Inc., Stratford CT, US |
| Decision | Substantially Equivalent, Jul 28, 1987 |
| Received | Jul 2, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872597
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.