Medical Device Recalls
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1 result found
510(K) Number: K111213 |
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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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Vision One Laser System Model GA-0025020, Serial No: 10050, 10051, 10053. Intended for use in the... | 2 | 09/11/2013 | Lumenis, Inc. |
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