510(k) K800096 ยท JAF Monitor, Ultrasonic, Nonfetal
AMBIVASON DR-200
| Applicant | Kt Medical, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 11, 1980 |
| Received | Jan 14, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800096
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.