Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K001725 |
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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 HeartStart XL Defibrillator/Monitor (Model number M4735A) - Product Usage: is for use in the... | 2 | 05/20/2020 | Philips North America, LLC |
Philips HeartStart XL, Model M4735A Defibrillator/Monitor | 2 | 12/18/2002 | Philips Medical Systems, Inc. Cardiac & Monitoring Systems |
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