K-number	K191881
Device name	KBL 7000 alpha hybridSun, KBL 7900 alpha hybridSun, KBL 8000 alpha hybridSun
Applicant	Kbl GmbH
Product code	LEJ
Device class	Class II
Decision date	Oct 28, 2019
Decision	Substantially Equivalent
Regulation	878.4635

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Source

View the full FDA submission: accessdata.fda.gov

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KBL 7000 alpha hybridSun, KBL 7900 alpha hybridSun, KBL 8000 alpha hybridSun

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