Class Class II

Remanufactured EndoWrist Cobra Grasper (420190) (K250417)

K250417 2025-08-20 Traditional
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Description

Remanufactured EndoWrist Cobra Grasper (420190) by Rebotix, an FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250417
Clearance Date2025-08-20
Clearance TypeTraditional
Product CodeQSM
Regulation Number876.1500

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