Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K133358 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system GYC4DD-1: The Nidek Green La... | 2 | 07/14/2015 |
FEI # 2936921 Nidek Inc |
| Endophotocoagulation Delivery 4EP-1 of GYC-1000 Green Laser Photocoagulator System; GYC4EP-01 0W02 ... | 2 | 07/14/2015 |
FEI # 2936921 Nidek Inc |
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