K-number	K862251
Device name	MODIFIED BIO-FLOW MODEL 200 URINE FLOW DEVICE
Applicant	Bio-Flow, Inc.
Product code	KNX
Device class	Class II
Decision date	Sep 4, 1986
Decision	Substantially Equivalent
Regulation	876.5250

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View the full FDA submission: accessdata.fda.gov

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MODIFIED BIO-FLOW MODEL 200 URINE FLOW DEVICE

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