510(k) K961374 ยท OWB Interventional Fluoroscopic X-Ray System
PHILIPS MULTIDIAGNOST 4
| Applicant | Philips Medical Systems, Inc., Da Best, NL |
| Decision | Substantially Equivalent, Aug 19, 1996 |
| Received | Apr 9, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961374
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 24, 2009 | Philips Medical Systems North America Co. Phillips MultiDiagnost MD4 Terminated |
JAA | None listed |
| May 6, 2006 | Philips Medical Systems North America Co. Phillips MD4 X-ray system Terminated |
JAA | None listed |
| Feb 27, 2003 | Philips Medical Systems MultiDiagnost 4 - x-ray system, multi functional/universal system for general use. Terminated |
JAA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.