510(k) K933791 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
PHILIPS ANGIOPRO RELEASE 2.1
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Nov 22, 1993 |
| Received | Aug 4, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933791
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.