510(k) K902542 ยท IZI System, X-Ray, Angiographic
PHILIPS INTEGRIS C2000 SYSTEM
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Aug 17, 1990 |
| Received | Jun 6, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902542
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.