510(k) K973857 ยท JAF Monitor, Ultrasonic, Nonfetal
FLOSTAT VASCULAR REPORT GENERATOR (VRG)
| Applicant | Biomedix, Inc., Camden NJ, US |
| Decision | Substantially Equivalent, Dec 29, 1997 |
| Received | Oct 9, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973857
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.