K-number	K124062
Device name	QDC-PRO, AND NOX-RIP
Applicant	Nox Medical
Product code	MNR
Device class	Class II
Decision date	Jul 10, 2013
Decision	Substantially Equivalent
Regulation	868.2375

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Source

View the full FDA submission: accessdata.fda.gov

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QDC-PRO, AND NOX-RIP

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