Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K905703 |
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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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Krupin Eye Valve, P/N 6003 | 2 | 05/06/2006 | Eagle Vision Inc |
Valve-EV Glaucoma Ultra-Smooth, P/N 6006 | 2 | 05/06/2006 | Eagle Vision Inc |
Glaucoma Aqueous Shunt 365 mm, valved, P/N EG365V | 2 | 05/06/2006 | Eagle Vision Inc |
Glaucoma Aqueous Shunt, 209 mm, valved, P/N EG209V | 2 | 05/06/2006 | Eagle Vision Inc |
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