510(k) K020055 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
PHILIPS INTEGRIS ALLURA 9 WITH FD OPTION
| Applicant | Philips Medical Systems, Bothell WA, US |
| Decision | Substantially Equivalent, Mar 15, 2002 |
| Received | Jan 8, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020055
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| 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.