510(k) K862805 ยท GDM Needle, Aspiration And Injection, Reusable
ANGIOMED VAC-U-CUT BIOPSY NEEDLE
| Applicant | Angiomed U.S., Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, Sep 29, 1986 |
| Received | Jul 22, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862805
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.