K-number	K864259
Device name	MODIFIED LASERFLO BLOOD PERFUSION MONITOR
Applicant	Tsi, Inc.
Product code	DPW
Device class	Class II
Decision date	Feb 20, 1987
Decision	Substantially Equivalent
Regulation	870.2100

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View the full FDA submission: accessdata.fda.gov

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MODIFIED LASERFLO BLOOD PERFUSION MONITOR

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