PHILIPS MEDICAL SYSTEMS
109 FDA 510(k) clearances · Recalling firm
◉ Watch PHILIPS MEDICAL SYSTEMS
| Record | Firm | Date |
|---|---|---|
| Easy Access PACS System with software Release 5, 6.2, or 7.2 recall (Z-1223-03) | Philips Medical Systems | 2003-09-12 |
| Gyroscan ACS-NT with software versions R6x, R7x, R8x recall (Z-1227-03) | Philips Medical Systems | 2003-09-12 |
| Gyroscan NT-Intera recall (Z-1228-03) | Philips Medical Systems | 2003-09-12 |
| Gyroscan Intera 1.0T & 1.5T recall (Z-1229-03) | Philips Medical Systems | 2003-09-12 |
| Model M4735A HeartStart XL Defibrillator//Monitor recall (Z-1226-03) | Philips Medical Systems | 2003-09-11 |
| Easy Access Software releases 1.1, 5.2, 6.2 & 7.2 recall (Z-1125-03) | Philips Medical Systems | 2003-08-12 |
| EasyWeb recall (Z-1128-03) | Philips Medical Systems | 2003-08-12 |
| MultiDiagnost 4 - x-ray system, multi functional/universal system for general use. recall (Z-0586-03) | Philips Medical Systems | 2003-02-27 |
| Philips BV300 Mobile X-Ray System recall (Z-0526-03) | Philips Medical Systems | 2003-02-01 |
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Every clearance here is in the API, with alerts when new ones post.