K-number	K211901
Device name	MolecuLightDX
Applicant	MolecuLight, Inc.
Product code	QJF
Device class	Class II
Decision date	Jul 21, 2021
Decision	Substantially Equivalent
Regulation	878.4550

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Source

View the full FDA submission: accessdata.fda.gov

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MolecuLightDX

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