Medical Device Recalls
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1 result found
510(K) Number: K170171 |
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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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Carl Zeiss Meditec AG, Goeschwitzer Strasse 51-52 07745 Jena, Germany, IOLMaster 700, REF 1932-169 ... | 2 | 10/15/2018 | Carl Zeiss Meditec AG |
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