Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K083517 |
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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 IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended for monitoring and record... | 2 | 12/08/2020 | Philips North America Llc |
Philips M8102A IntelliVue MP2 Model: 865040 Indicated for use by health care professionals wheneve... | 2 | 09/29/2010 | Philips Healthcare Inc. |
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