Medical Device Recalls
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1 result found
510(K) Number: K091010 |
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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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Instructions for Use for the blue endo MOREsolution Electromechanical Laparoscopic Morcellator Syste... | 2 | 08/02/2014 | Market-Tiers Inc |
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