K-number	K945806
Device name	SILICATH ALL SILICONE FOLEY CATHETER
Applicant	Unomedical Sdn Bhd
Product code	EZL
Device class	Class II
Decision date	Mar 21, 1995
Decision	Substantially Equivalent
Regulation	876.5130

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View the full FDA submission: accessdata.fda.gov

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SILICATH ALL SILICONE FOLEY CATHETER

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