510(k) K943989 ยท HFO Recorder, Pressure, Intrauterine
LAPAROSCOPIC/ENDOSCOPIC INSTRUEMENT
| Applicant | Gabris Surgical Corp., Virginia Beach VA, US |
| Decision | Substantially Equivalent, Sep 12, 1994 |
| Received | Aug 16, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943989
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.