510(k) K900893 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
CARDIOVUE CFS-100
| Applicant | Bv Medical Equipment Co., Hanover MD, US |
| Decision | Substantially Equivalent, Apr 19, 1990 |
| Received | Feb 27, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900893
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.