Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K123429 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Gyrus ACMI Diego Elite Tubeset, intended for cutting, coagulation, drilling, debriding, and removal ... | 2 | 06/11/2015 | Gyrus Acmi, Incorporated |
Gyrus ACMI Diego Elite Tubeset; intended for cutting, coagulation, drilling, debriding, and removal ... | 2 | 06/11/2015 | Gyrus Acmi, Incorporated |
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