Medical Device Recalls
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1 result found
510(K) Number: K031920 |
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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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Pioneer Catheter (Crosspoint TransAccess Catheter); Model TA-XP-001; Product is manufactured and di... | 2 | 11/22/2006 | Medtronic Vascular |
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