K-number	K231959
Device name	EXPD 4357; EXPD 4357P
Applicant	DRTECH Corporation
Product code	MQB
Device class	Class II
Decision date	Aug 1, 2023
Decision	Substantially Equivalent
Regulation	892.1680

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Source

View the full FDA submission: accessdata.fda.gov

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EXPD 4357; EXPD 4357P

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