K-number	K200134
Device name	Jimushi Sterile Urethral Catheter for single use
Applicant	Hangzhou Jimushi Meditech Co., Ltd.
Product code	GBM
Device class	Class II
Decision date	Jun 1, 2020
Decision	Substantially Equivalent
Regulation	876.5130

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Source

View the full FDA submission: accessdata.fda.gov

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Jimushi Sterile Urethral Catheter for single use

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