K-number	K780167
Device name	CATH KIT, URINE SPECIMEN
Applicant	C.R. Bard, Inc.
Product code	FMH
Device class	Class I
Decision date	Feb 21, 1978
Decision	Substantially Equivalent
Regulation	864.3250

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View the full FDA submission: accessdata.fda.gov

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CATH KIT, URINE SPECIMEN

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