Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K151706 |
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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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SPECULAR MICROSCOPE CEM-530; Software version 1.08 and 1.09. Opthalmic: The NIDEK Specular Micros... | 2 | 09/01/2016 | Nidek Inc |
NIDEK Specular Microscope, Model CEM-530 - Product Usage: The device provides noncontact, high magni... | 3 | 01/02/2020 | Nidek, Inc. |
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