Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K093392 |
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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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Exodus(TM) 8F (2.7 mm)/ 35 cm Standard Loop Biliary Drainage Catheter with Hydrophilic Coating, REF/... | 2 | 01/11/2012 | Navilyst Medical, Inc |
Exodus(TM) 10 F (3.4 mm)/ 35 cm Standard Loop Biliary Drainage Catheter with Hydrophilic Coating, RE... | 2 | 01/11/2012 | Navilyst Medical, Inc |
Exodus(TM) 8F (2.7 mm)/25 cm Standard Loop Multipurpose Drainage Catheter with Hydrophilic Coating, ... | 2 | 10/07/2010 | Navilyst Medical, Inc |
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