510(k) K943200 ยท JAF Monitor, Ultrasonic, Nonfetal
FLOSCOPE SUPER VASCULAR LAB
| Applicant | Advance Medical Device, Inc., Camden NJ, US |
| Decision | Substantially Equivalent, Nov 21, 1995 |
| Received | Jul 5, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943200
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.