K-number	K230754
Device name	L12 LED Light Source with AIM
Applicant	Stryker
Product code	OWN
Device class	Class II
Decision date	Apr 11, 2023
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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L12 LED Light Source with AIM

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