510(k) K904012 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
PHILIPS INTEGRIS I 2000 SYSTEM
| Applicant | Philips Medical Systems, Inc., 5680 Da Best, NL |
| Decision | Substantially Equivalent, Nov 29, 1990 |
| Received | Aug 29, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904012
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 6, 2006 | Philips Medical Systems North America Co. Phillips MD3 X-ray system Terminated |
JAA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.