K-number	K896053
Device name	ALL SILICONE FOLEY CATHETER
Applicant	Rochester Medical Corp.
Product code	KOD
Device class	Class II
Decision date	Feb 12, 1990
Decision	Substantially Equivalent
Regulation	876.5130

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View the full FDA submission: accessdata.fda.gov

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ALL SILICONE FOLEY CATHETER

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