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FDA 510(k)

KYMCO EQ10D Scooter

K-Number: K163201 · 2017-03-16

ApplicantKwang Yang Motor Co., Ltd.
Decision Date2017-03-16
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KYMCO EQ10D Scooter is a medical device manufactured by Kwang Yang Motor Co., Ltd.. It received FDA 510(k) clearance on 2017-03-16 under approval number K163201. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KYMCO EQ10D Scooter?

KYMCO EQ10D Scooter is a medical device that received FDA 510(k) clearance on 2017-03-16. It is manufactured by Kwang Yang Motor Co., Ltd.. The 510(k) number is K163201.

When was KYMCO EQ10D Scooter approved by the FDA?

KYMCO EQ10D Scooter received FDA 510(k) clearance on 2017-03-16, under approval number K163201.

What company makes KYMCO EQ10D Scooter?

KYMCO EQ10D Scooter is manufactured by Kwang Yang Motor Co., Ltd..

What is the FDA product code for KYMCO EQ10D Scooter?

The FDA product code for KYMCO EQ10D Scooter is INI.

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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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