Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K141079 |
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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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OptiMedica Catalys Precision Laser System, CE 0044 containing software cOS 5.00.33 Product Label ... | 2 | 10/03/2018 | Johnson & Johnson Surgical Vision Inc |
Catalys Precision Laser System-Catalys - U - US product; Catalys-1 - International product; software... | 2 | 05/28/2015 | Optimedica Corporation |
OptiMedica Catalys Precision Laser System; Model No(s). Catalys-U (US), and Catalys-I (Outside US). ... | 2 | 04/23/2015 | Abbott Medical Optics, Inc. |
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