K-number	K222767
Device name	PeekMed web (v1)
Applicant	Peek Health, S.A.
Product code	LLZ
Device class	Class II
Decision date	Dec 30, 2022
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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PeekMed web (v1)

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