K-number	K014025
Device name	HOMMED SENTRY III PATIENT MONITOR SYSTEM WITH CARD READER
Applicant	Hommed, LLC
Product code	DQA
Device class	Class II
Decision date	Apr 9, 2002
Decision	Substantially Equivalent
Regulation	870.2700

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Source

View the full FDA submission: accessdata.fda.gov

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HOMMED SENTRY III PATIENT MONITOR SYSTEM WITH CARD READER

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