Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K120476 |
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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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MACROLYTE Premie Dispersive Electrode, REF 440-2400, CONMED CORPORATION. The device is applied to ... | 2 | 06/04/2014 | ConMed Corporation |
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures. | 3 | 09/16/2019 | CooperSurgical, Inc. |
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