Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K972484 |
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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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6F Viking Guiding Catheter, Percutaneous catheter Shape BP-L, Part Number: 1001970-06, Abbott Vascul... | 3 | 08/13/2008 | Abbott Vascular-Cardiac Therapies dba Guidant Corporation |
6F Viking Guiding Catheter, Percutaneous catheter, Shape ALR 1.2, Part Number: 1001934-06, Abbott Va... | 3 | 08/13/2008 | Abbott Vascular-Cardiac Therapies dba Guidant Corporation |
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