K-number	K100020
Device name	DX SERIES FINGER SENSOR
Applicant	Dixtal Medical, Inc.
Product code	DQA
Device class	Class II
Decision date	Mar 8, 2010
Decision	Substantially Equivalent
Regulation	870.2700

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Source

View the full FDA submission: accessdata.fda.gov

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DX SERIES FINGER SENSOR

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