Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K100272 |
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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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Philips Medical: 865047 IntelliVue Clinical Information Portfolio Release D.03 865209 IntelliVue C... | 2 | 08/31/2011 | Philips Healthcare Inc. |
Philips IntelliVue Clinical Information Portfolio software as follows: 865047 IntelliVue Clinical I... | 2 | 05/10/2011 | Philips Healthcare Inc. |
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