510(k) K954596 ยท FCG Biopsy Needle
PRO-B CORE-RECT COAXIAL BIOPSY SYSTEM
| Applicant | Promedical , Ltd., Wyckoff NJ, US |
| Decision | Substantially Equivalent, Oct 7, 1995 |
| Received | Oct 3, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954596
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.