Medical Device Recalls
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1 result found
510(K) Number: K161092 |
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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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| GalaSHAPE 3D; product code SH3D03, a medium size oval GalaSHAPE" 3D is indicated for use as a biore... | 2 | 01/05/2017 |
FEI # 3005670760 Tepha Incorporated |
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