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FDA 510(k)

Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III)

K-Number: K190118 · 2020-05-13

ApplicantGuangzhou Xinbo Electronic Co., Ltd.
Decision Date2020-05-13
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III) is a medical device manufactured by Guangzhou Xinbo Electronic Co., Ltd.. It received FDA 510(k) clearance on 2020-05-13 under approval number K190118. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III)?

Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III) is a medical device that received FDA 510(k) clearance on 2020-05-13. It is manufactured by Guangzhou Xinbo Electronic Co., Ltd.. The 510(k) number is K190118.

When was Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III) approved by the FDA?

Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III) received FDA 510(k) clearance on 2020-05-13, under approval number K190118.

What company makes Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III)?

Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III) is manufactured by Guangzhou Xinbo Electronic Co., Ltd..

What is the FDA product code for Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III)?

The FDA product code for Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III) is GXY.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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