K-number	K220969
Device name	GelPOINT V-Path Vaginal Access System
Applicant	Applied Medical Resources Corporation
Product code	MOK
Device class	Class II
Decision date	Sep 16, 2022
Decision	Substantially Equivalent
Regulation	884.1630

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Source

View the full FDA submission: accessdata.fda.gov

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GelPOINT V-Path Vaginal Access System

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