K-number	K212077
Device name	Teleflex Rusch SoftSimplastic Foley Catheters
Applicant	Teleflexmedical, Inc.
Product code	EZL
Device class	Class II
Decision date	Jul 27, 2023
Decision	Substantially Equivalent
Regulation	876.5130

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Source

View the full FDA submission: accessdata.fda.gov

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Teleflex Rusch SoftSimplastic Foley Catheters

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