K-number	K183169
Device name	Pulse 2.0, Pulse Pro 2.0
Applicant	NormaTec Industries, LP
Product code	IRP
Device class	Class II
Decision date	Dec 27, 2018
Decision	Substantially Equivalent
Regulation	890.5650

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Source

View the full FDA submission: accessdata.fda.gov

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Pulse 2.0, Pulse Pro 2.0

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