Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K132304 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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EPIQ 7 Ultrasound System, Model 795200, 795201, 795202. Intended for diagnostic ultrasound imagin... | 2 | 11/20/2013 | Philips Medical Systems North America Inc. |
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