510(k) K961782 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
BIO-BINKI
| Applicant | Biomni Medical Systems, Inc., Lehi UT, US |
| Decision | Substantially Equivalent, Mar 28, 1997 |
| Received | May 8, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961782
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.