510(k) K942484 ยท FHO Pneumoperitoneum Needle
VERRES NEEDLE
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Jun 24, 1994 |
| Received | May 25, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942484
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.