K-number	K221796
Device name	Cyware 4H and Cysart 4H
Applicant	Abys Medical
Product code	LLZ
Device class	Class II
Decision date	Dec 30, 2022
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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Cyware 4H and Cysart 4H

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