510(k) K923813 ยท IZI System, X-Ray, Angiographic
PHILIPS INTEGRIS V3000 ROTATIONAL ANGIO FUNCTION
| Applicant | Philips Medical Systems, Inc., 5680 Da Best, NL |
| Decision | Substantially Equivalent, Oct 16, 1992 |
| Received | Jul 29, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923813
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 20, 2004 | Philips Medical Systems Sales & Service Region No. America Monitor Ceiling Suspension for Fluoroscopic and Angiographic X-Ray Systems. Terminated |
IZI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.