Philips Medical Systems North America Inc.
5 FDA 510(k) clearances · Recalling firm
◉ Watch Philips Medical Systems North America Inc.
| Record | Firm | Date |
|---|---|---|
| Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound imaging and flu recall (Z-1263-2014) | Philips Medical Systems North America Inc. | 2014-03-20 |
| Philips Model EPIQ 7 Ultrasound System. Intended for diagnostic ultrasound imaging and flu recall (Z-1264-2014) | Philips Medical Systems North America Inc. | 2014-03-20 |
| Philips HeartStart FR3 Automated External Defibrillator (AED), models 861388 and 861389. T recall (Z-1225-2014) | Philips Medical Systems North America Inc. | 2014-03-19 |
| Philips HeartStart Home and OnSite (HS1) automated external defibrillators (AEDs). Product recall (Z-1232-2014) | Philips Medical Systems North America Inc. | 2014-03-19 |
| EPIQ 7 Ultrasound System, Model 795200, 795201, 795202. Intended for diagnostic ultrasound recall (Z-0368-2014) | Philips Medical Systems North America Inc. | 2013-11-20 |
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Every clearance here is in the API, with alerts when new ones post.