K-number	K233998
Device name	TRAQinform IQ
Applicant	Aiq Global, Inc.
Product code	LLZ
Device class	Class II
Decision date	Sep 5, 2024
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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TRAQinform IQ

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