Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K011093 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Viridia/Agilent Information Center Model : M3150A#C01 | 2 | 02/28/2003 | Philips Medical Systems, Inc. Cardiac & Monitoring Systems |
Intellivue Information Center Model: M3150BU#CO1 | 2 | 02/28/2003 | Philips Medical Systems, Inc. Cardiac & Monitoring Systems |
Intellivue Information Center Model: M3150B#C01 | 2 | 02/28/2003 | Philips Medical Systems, Inc. Cardiac & Monitoring Systems |
Viridia/Agilent Information Center Model : M3151A#CO1 | 2 | 02/28/2003 | Philips Medical Systems, Inc. Cardiac & Monitoring Systems |
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