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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
PMA Number: P910001/S115
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Recall
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FDA Recall
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Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent upon device in use 1... 2 07/11/2022 FEI # 3007284006
Spectranetics Corporation
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