510(k) K010779 ยท FHO Pneumoperitoneum Needle
MODIFICATION TO:LAPAROSCOPIC/ENDOSCOPIC INSTRUMENT
| Applicant | Gibbons Surgical Corp., Virginia Beach VA, US |
| Decision | Substantially Equivalent, Apr 10, 2001 |
| Received | Mar 15, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K010779
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.