Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K131523 |
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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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C2 CryoBalloon Focal Catheter, REF FG-1009. C2 CryoBalloon Ablation System is used as a cryosurgica... | 2 | 06/05/2018 | PENTAX of America Inc |
C2 CryoBalloon Ablation System - Controller Cap. C2 CryoBalloon Controller; Cryosurgical Unit, Cryo... | 2 | 03/15/2017 | C2 Therapeutics, Inc. |
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