510(k) K760888 ยท KNG Monitor, Ultrasonic, Fetal
MODEL 6/60 CRT VIDEO-SONAR
| Applicant | Vexilar, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 1, 1977 |
| Received | Oct 26, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760888
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.