Class Class II

Single Use Electrosurgical Knife (KD-612L, KD-612U); Single Use Electrosurgical Knife (KD-620UR); Single Use Electrosurgical Knife (KD-650L, KD-650U) (K250351)

K250351 2025-10-10 Traditional
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Description

Single Use Electrosurgical Knife (KD-612L, KD-612U); Single Use Electrosurgical Knife (KD-620UR); Single Use Electrosurgical Knife (KD-650L, KD-650U) by Olympus Medical Systems Corporation, an FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250351
Clearance Date2025-10-10
Clearance TypeTraditional
Product CodeKNS
Regulation Number876.4300

FDA Database

View on FDA Database

Categories

Gastroenterology & Urology

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