510(k) K854404 ยท FCG Biopsy Needle
ROTEX SCREW BIOPSY NEEDLE
| Applicant | Meadox Surgimed, Inc., Oakland NJ, US |
| Decision | Substantially Equivalent, Dec 2, 1985 |
| Received | Nov 1, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854404
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.