510(k) K874585 ยท DWO Needle, Biopsy, Cardiovascular
ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE
| Applicant | Angiomed U.S., Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, Dec 2, 1987 |
| Received | Nov 9, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874585
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.