K-number	K233013
Device name	2-Way 100% Silicone Cleartract Catheter
Applicant	Silq Technologies Corporation
Product code	EZL
Device class	Class II
Decision date	Jan 23, 2024
Decision	Substantially Equivalent
Regulation	876.5130

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Source

View the full FDA submission: accessdata.fda.gov

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2-Way 100% Silicone Cleartract Catheter

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