Medical Device Recalls
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1 result found
510(K) Number: K101006 |
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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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WaveLight FS200 Femtosecond Laser System Alcon Product Code 8065990714 WaveLight Model 1025 Soft... | 2 | 05/25/2011 | Wavelight AG |
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