K-number	K183148
Device name	OKLand Patient Return Electrode Pad
Applicant	Auckland Medical Polymer(Tianjin) Co., Ltd.
Product code	GEI
Device class	Class II
Decision date	Feb 4, 2020
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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OKLand Patient Return Electrode Pad

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