K-number	K192234
Device name	ActiPatch
Applicant	Bioelectronics Corporation
Product code	PQY
Device class	Class II
Decision date	Jan 31, 2020
Decision	Substantially Equivalent
Regulation	890.5290

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Source

View the full FDA submission: accessdata.fda.gov

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ActiPatch

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