K-number	K223694
Device name	Tinearity G1 (6103); Tinearity G1 Adapters x3 (6042)
Applicant	Duearity AB
Product code	KLW
Device class	Class II
Decision date	Jun 30, 2023
Decision	Substantially Equivalent
Regulation	874.3400

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Source

View the full FDA submission: accessdata.fda.gov

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Tinearity G1 (6103); Tinearity G1 Adapters x3 (6042)

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