Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K083291 |
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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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Cirrus HD-OCT Model 4000 instruments, new and refurbished, distributed with, or upgraded to, version... | 2 | 05/02/2011 | Carl Zeiss Meditec Inc |
Cirrus HD-OCT Model 400 instruments; new and refurbished, with or upgraded to, version 4.6 or 5.1.0 ... | 2 | 05/02/2011 | Carl Zeiss Meditec Inc |
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