K-number	K231053
Device name	Unicare (K-UNICARE-USA)
Applicant	Tenscare, Ltd.
Product code	NUH
Device class	Class II
Decision date	Aug 18, 2023
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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Unicare (K-UNICARE-USA)

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