Medical Device Recalls
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1 result found
510(K) Number: K110415 |
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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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REF 42-411571 QTY 1 CATALOG CAUTION. SEE INSTRUCTIONS FOR USE SIGNATURE M PKA GDE/MDL SET SML-MP... | 2 | 01/03/2014 | Materialise USA LLC |
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