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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K210925
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Flexiva Pulse 242 Single-Use Laser Fibers-intended to be used as a device that transmits Ho:YAG lase... 2 07/21/2023 Boston Scientific Corporation
Flexiva Pulse 242 TracTip Single-Use Laser Fibers - intended to be used as a device that transmits H... 2 07/21/2023 Boston Scientific Corporation
Flexiva Pulse 242 TracTip Single-Use Laser Fibers -intended to be used as a device that transmits Ho... 2 07/21/2023 Boston Scientific Corporation
Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be used as a device that transmits Ho:YAG ... 2 07/21/2023 Boston Scientific Corporation
Flexiva Pulse ID-intended to be used as a device that transmits Ho:YAG laser energy from cleared las... 2 07/21/2023 Boston Scientific Corporation
Flexiva Pulse 242 ID Trac Single Use Fiber-intended to be used as a device that transmits Ho:YAG las... 2 07/21/2023 Boston Scientific Corporation
Flexiva Pulse ID-intended to be used as a device that transmits Ho:YAG laser energy from cleared las... 2 07/21/2023 Boston Scientific Corporation
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