Medical Device Recalls
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1 result found
510(K) Number: K150323 |
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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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The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser i... | 2 | 03/29/2018 | SIE AG, Surgical Instrument Engineering |
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