510(k) K900882 ยท JAF Monitor, Ultrasonic, Nonfetal
MULTI DOPPLEX, MD-1
| Applicant | Huntleigh Technology, Inc., Manalapan NJ, US |
| Decision | Substantially Equivalent, Aug 22, 1990 |
| Received | Feb 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900882
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.