Medical Device Recalls
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1 result found
510(K) Number: K960883 |
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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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Taut Intraducer Peritoneal Catheter, 12 Fr x 10 Fr x 20.3 cm; a sterile, Rx peritoneal catheter for... | 2 | 02/15/2007 | Taut, Inc. |
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