Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K081804 |
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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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Volcano Pioneer Plus Re-Entry Catheter; Product Code PPLUS20, Catheter for Crossing Total Occlusion... | 2 | 09/02/2015 | Volcano Corporation |
Pioneer Plus Catheter PPlus 120 dual lumen device, inserted through a 6F introducer sheath and plac... | 2 | 01/06/2011 | Medtronic CardioVascular |
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