Medical Device Recalls
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1 result found
510(K) Number: K142454 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Wall Chart for STERRAD 100NX System, P/N 10104. The STERRAD 100NX Sterilizer is designed for ster... | 2 | 08/13/2015 |
FEI # 3003662624 Advanced Sterilization Products |
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