Medical Device Recalls
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1 result found
510(K) Number: K033293 |
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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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ML 7090 Calibrated LASIK Blade (CLB); CLB CALIBRATED LASIK BLADE 10. ML 7090 Calibrated LASIK Bla... | 2 | 03/13/2015 | Med-logics Inc |
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