510(k) K912470 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
PHILIPS DIAGNOST 96
| Applicant | Philips Medical Systems, Inc., 5680 Da Best, NL |
| Decision | Substantially Equivalent, Aug 7, 1991 |
| Received | Jun 4, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912470
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 8, 2011 | Philips Healthcare Inc. Philips Diagnost 94, Diagnost 96, Diagnost 97 Universal X-Ray System
The Diagnost is a multifunctional, universal X~ray system with remote controlled facilities. Routine examinations that can be per Terminated |
JAA | None listed |
| Jul 20, 2004 | Philips Medical Systems Sales & Service Region No. America Diagnost 97 Terminated |
None listed | |
| 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 |
| Sep 12, 2003 | Philips Medical Systems Diagnost 94 Terminated |
IZZ | None listed |
| Sep 12, 2003 | Philips Medical Systems Multidiagnost 96 Terminated |
IZZ | None listed |
| Sep 12, 2003 | Philips Medical Systems Multidiagnost 97 Terminated |
IZZ | None listed |
| Sep 11, 2003 | Philips Medical Systems Sales & Service Region No. America Diagnost 96 Terminated |
IZZ | None listed |
| Sep 11, 2003 | Philips Medical Systems Sales & Service Region No. America Diagnost 97 Terminated |
IZZ | None listed |
| Sep 11, 2003 | Philips Medical Systems Sales & Service Region No. America Diagnost 94 Terminated |
IZZ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.