510(k) K943338 ยท JAF Monitor, Ultrasonic, Nonfetal
BIOSENSOR BIDOP VASCULAR TEST SYSTEM
| Applicant | Biosensor Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 12, 1996 |
| Received | Jul 12, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943338
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.