Class Class II

Revolve Surgical System (K243968)

K243968 2025-10-03 Traditional
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Description

Revolve Surgical System by Revolve Surgical, Inc., an FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243968
Clearance Date2025-10-03
Clearance TypeTraditional
Product CodeGCJ
Regulation Number876.1500

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