K-number	K213370
Device name	VERIQA
Applicant	Ptw-Freiburg Physikalisch-Technische-Werkstaetten
Product code	IYE
Device class	Class II
Decision date	Mar 30, 2022
Decision	Substantially Equivalent
Regulation	892.5050

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View the full FDA submission: accessdata.fda.gov

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VERIQA

Everything you need for a 510(k) submission. Nothing you don't.