K-number	DEN200019
Device name	Oxehealth Vital Signs
Applicant	Oxehealth Limited
Product code	QME
Device class	Class II
Decision date	Mar 26, 2021
Decision	Not Substantially Equivalent
Regulation	870.2785

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Source

View the full FDA submission: accessdata.fda.gov

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Oxehealth Vital Signs

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