Medical Device Recalls
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1 result found
510(K) Number: K093232 |
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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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Greatbatch OptiSeal Valved PTFE Peelable Introducer, Model 1000093-001, 1000093-002, 1000093-003, 1... | 2 | 08/27/2010 | Greatbatch Medical |
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