510(k) K910855 ยท FHP Needle, Pneumoperitoneum, Simple
ENDOPATH VERESS NEEDLE
| Applicant | Symbiosis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Apr 18, 1991 |
| Received | Feb 28, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910855
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.