K-number	K231011
Device name	Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulse
Applicant	Meridian AG
Product code	HQF
Device class	Class II
Decision date	Sep 12, 2023
Decision	Substantially Equivalent
Regulation	886.4390

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Source

View the full FDA submission: accessdata.fda.gov

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Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulse

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