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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ADULT/CHILD Radiotranslucent Electrode, Part number T100AC-PHILIPS, Rx ONLY, For use with Philips He... | 1 | 12/24/2014 | Heart Sync, Inc. |
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