Medical Device Recalls
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1 result found
510(K) Number: K936181 |
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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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Midmark M11 Ultra Steam Sterilizer, Distributed by: Midmark Corporation, 60 Vista Drive, Versailles,... | 2 | 01/11/2012 | Midmark Corportation |
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