Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K081983 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Philips Audio-Video Engineering PAS-210 Remote Active Speakers Kit used with the IntelliVue Informat... | 2 | 05/19/2011 |
FEI # 1218950 Philips Healthcare Inc. |
| Physiological Monitoring, Patient Monitor M31250 Information Center Local Database Releases A, B, ... | 2 | 01/27/2011 |
FEI # 1218950 Philips Healthcare Inc. |
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