K-number	K170926
Device name	BrainPulse 1100
Applicant	Jan Medical, Inc.
Product code	POP
Device class	Class II
Decision date	Apr 28, 2017
Decision	Substantially Equivalent
Regulation	882.1630

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Source

View the full FDA submission: accessdata.fda.gov

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BrainPulse 1100

Everything you need for a 510(k) submission. Nothing you don't.