Medical Device Recalls
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1 result found
510(K) Number: K100019 |
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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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PASCAL and PASCAL Streamline (532 nm.577 nm); Treats the patient's eye. | 2 | 07/19/2013 | Topcon Medical Laser Systems, Inc |
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