K-number	K193031
Device name	EXPD 4343P, EXPD 3643P
Applicant	DRTECH Corporation
Product code	MQB
Device class	Class II
Decision date	Nov 22, 2019
Decision	Substantially Equivalent
Regulation	892.1680

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Source

View the full FDA submission: accessdata.fda.gov

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EXPD 4343P, EXPD 3643P

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