Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K080421 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Medstorm Adult Radiolucent Electrode Philips Medical , Part #16250, HeartSync Ann Arbor, MI. Th... | 2 | 02/18/2011 | Heart Sync, Inc |
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