K-number	K230926
Device name	Ova+ (K-OVAP-USA)
Applicant	Tenscare, Ltd.
Product code	NUH
Device class	Class II
Decision date	Dec 15, 2023
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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Ova+ (K-OVAP-USA)

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