K-number	K192453
Device name	DIAMOND-5A/6A/8A
Applicant	DRGEM Corporation
Product code	KPR
Device class	Class II
Decision date	Oct 1, 2019
Decision	Substantially Equivalent
Regulation	892.1680

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Source

View the full FDA submission: accessdata.fda.gov

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DIAMOND-5A/6A/8A

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