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FDA 510(k)

Scooter (PS30)

K-Number: K242628 · 2024-12-20

ApplicantLichtmega Technology Co., Ltd.
Decision Date2024-12-20
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Scooter (PS30) is a medical device manufactured by Lichtmega Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-12-20 under approval number K242628. 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 Scooter (PS30)?

Scooter (PS30) is a medical device that received FDA 510(k) clearance on 2024-12-20. It is manufactured by Lichtmega Technology Co., Ltd.. The 510(k) number is K242628.

When was Scooter (PS30) approved by the FDA?

Scooter (PS30) received FDA 510(k) clearance on 2024-12-20, under approval number K242628.

What company makes Scooter (PS30)?

Scooter (PS30) is manufactured by Lichtmega Technology Co., Ltd..

What is the FDA product code for Scooter (PS30)?

The FDA product code for Scooter (PS30) is INI.

Other Devices by Lichtmega Technology Co., Ltd.

K241460Manual Wheelchair

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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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