Medical Device Recalls
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1 result found
510(K) Number: K133132 |
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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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OPTICAL BIOMETER AL-Scan: Software Version: 1.09 and earlier. Ophthalmic: The OPTICAL BIOMETER AL... | 2 | 08/18/2016 | Nidek Inc |
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