Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K041674 |
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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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M3811B Philips Telemonitoring Clinical Review Software part of Philips Telemonitoring System, M3810A... | 2 | 10/10/2008 | Philips Medical Systems |
Philips Telemonitoring System Software (M3811B) used with Philips Telemonitoring System (M3810B) ... | 3 | 09/18/2008 | Philips Medical Systems |
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