510(k) K912925 ยท JAF Monitor, Ultrasonic, Nonfetal
ULTRA PVD
| Applicant | Advanced Medical Products, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jun 18, 1992 |
| Received | Jul 3, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912925
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.