Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K063375 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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HeartStart MRx Monitor/Defibrillator; Model. Numbers: M3535A, M3536A, M3536J, M3536M, M3536MC, M3536... | 2 | 01/13/2015 | Philips Medical Systems, Inc. |
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