K-number	K183328
Device name	Pulse Rx 2.0, Pulse Pro Rx 2.0
Applicant	NormaTec Industries, LP
Product code	JOW
Device class	Class II
Decision date	Dec 21, 2018
Decision	Substantially Equivalent
Regulation	870.5800

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Source

View the full FDA submission: accessdata.fda.gov

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Pulse Rx 2.0, Pulse Pro Rx 2.0

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