Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K110622 |
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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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Lithium Ion Battery M4605A and M4607A for use with IntelliVue Patient Monitors. The monitor is use... | 2 | 05/16/2014 | Philips Medical Systems, Inc. |
Philips IntelliVue Patient Monitors: The monitor is intended to be used for monitoring and recordi... | 2 | 03/01/2012 | Philips Healthcare Inc. |
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