Medical Device Recalls
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1 result found
510(K) Number: K140933 |
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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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Alive ECG App 2.1.2 ( a medical device application for the Apple iOS operating system, intended to b... | 3 | 02/18/2015 | Alivecor SFO |
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