K-number	K812005
Device name	CAPILLARY PERFUSION MONITOR #LD5000
Applicant	Nuclear Pacific, Inc.
Product code	DPW
Device class	Class II
Decision date	Feb 4, 1982
Decision	Substantially Equivalent
Regulation	870.2100

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View the full FDA submission: accessdata.fda.gov

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CAPILLARY PERFUSION MONITOR #LD5000

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