510(k) K921101 ยท IZI System, X-Ray, Angiographic
PHILIPS INTEGRIS V3000 FILM
| Applicant | Philips Medical Systems, Inc., 5680 Da Best, NL |
| Decision | Substantially Equivalent, May 15, 1992 |
| Received | Mar 9, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921101
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.