Medical Device Recalls
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1 result found
510(K) Number: K182010 |
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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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| progenamatrix Human Keratin Matrix, sterile, Rx, with the following model numbers: (1) PM2012, 12 x ... | 2 | 05/26/2022 | ProgenaCare |
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