Medical Device Recalls
-
1 to 4 of 4 Results
510(K) Number: K122418 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
IOL Master 5.5: Software versions 7.5 and 7.7; Ophthalmic: used to obtain ocular measurements and... | 2 | 12/01/2015 | Carl Zeiss Meditec AG |
IOL Master 500: Software versions 7.5 and 7.7; Ophthalmic: IOL Master 500 is intended for biometr... | 2 | 12/01/2015 | Carl Zeiss Meditec AG |
Zeiss brand IOLMaster, Version 1-5, Biomicroscope, Slit-Lamp, AC-Powered, Product is manufacture... | 2 | 11/15/2013 | Carl Zeiss Meditec, Inc. |
Zeiss brand IOLMaster 500, Model 500, Biomicroscope, Slit-Lamp, AC-Powered, Product is manufactu... | 2 | 11/15/2013 | Carl Zeiss Meditec, Inc. |
-