510(k) K925302 ยท IZF System, X-Ray, Tomographic
PHILIPS INTEGRIS H/HM SYSTEM
| Applicant | Philips Medical Systems, Inc., 5680 Da Best, NL |
| Decision | Substantially Equivalent, Dec 17, 1992 |
| Received | Oct 21, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925302
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 21, 2018 | Philips Electronics North America Corporation Poly C- DMCP-Visub(H3000), System Code 72238
Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions Terminated |
IZF | None listed |
| Sep 21, 2018 | Philips Electronics North America Corporation Cesar-DMCP-Visub(HM2000/3000), System Code 72239
Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions Terminated |
IZF | None listed |
| Sep 21, 2018 | Philips Electronics North America Corporation Cesar Powerpack-Visub(V3000), System Code 72243
Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions Terminated |
IZF | None listed |
| Nov 29, 2005 | Philips Medical Systems North America Co. Phillips AD5 table for use with Integris and Integris Allura x-ray systems Terminated |
IZI | None listed |
| Nov 29, 2005 | Philips Medical Systems North America Co. Phillips AD6 table for use with Integris and Integris Allura x-ray systems. The AD6 is the tilt version. Terminated |
IZI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.