Medical Device Recalls
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1 result found
510(K) Number: K091540 |
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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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| MTD 4000 - Mettler Traction Decompression System, Model: ME 4000 Product Usage: Provide traction... | 2 | 06/17/2011 |
FEI # 2013558 Mettler Electronics Corp |
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