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FDA 510(k)

OKLand Patient Return Electrode Pad

K-Number: K183148 · 2020-02-04

ApplicantAuckland Medical Polymer(Tianjin) Co., Ltd.
Decision Date2020-02-04
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OKLand Patient Return Electrode Pad is a medical device manufactured by Auckland Medical Polymer(Tianjin) Co., Ltd.. It received FDA 510(k) clearance on 2020-02-04 under approval number K183148. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OKLand Patient Return Electrode Pad?

OKLand Patient Return Electrode Pad is a medical device that received FDA 510(k) clearance on 2020-02-04. It is manufactured by Auckland Medical Polymer(Tianjin) Co., Ltd.. The 510(k) number is K183148.

When was OKLand Patient Return Electrode Pad approved by the FDA?

OKLand Patient Return Electrode Pad received FDA 510(k) clearance on 2020-02-04, under approval number K183148.

What company makes OKLand Patient Return Electrode Pad?

OKLand Patient Return Electrode Pad is manufactured by Auckland Medical Polymer(Tianjin) Co., Ltd..

What is the FDA product code for OKLand Patient Return Electrode Pad?

The FDA product code for OKLand Patient Return Electrode Pad is GEI.

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Official Source

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