510(k) K950708 ยท KXO Monitor, Pressure, Intrauterine
LIFETRACE INTRAUTERINE PRESSURE CATHETER IUP 3000
| Applicant | Graphic Controls Corp., Buffalo NY, US |
| Decision | Substantially Equivalent, May 25, 1995 |
| Received | Feb 13, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950708
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.