K-number	K160608
Device name	NormaTec Pulse and NormaTec Pulse Pro
Applicant	NormaTec Industries, LP
Product code	IRP
Device class	Class II
Decision date	Apr 13, 2016
Decision	Substantially Equivalent
Regulation	890.5650

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Source

View the full FDA submission: accessdata.fda.gov

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NormaTec Pulse and NormaTec Pulse Pro

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