Class Class II

Triopsy Actuator (TMSDGB); Triopsy Biopsy Needle (BN-1825-36-01); Triopsy Biopsy Needle (BN-1825-55-01) (K242228)

K242228 2025-01-10 Traditional
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Description

Triopsy Actuator (TMSDGB); Triopsy Biopsy Needle (BN-1825-36-01); Triopsy Biopsy Needle (BN-1825-55-01) by Triopsy Medical, Inc., an FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242228
Clearance Date2025-01-10
Clearance TypeTraditional
Product CodeKNW
Regulation Number876.1075

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