eFOLDi Scooter, Lite

FDA 510(k) K223492 · Suntech UK , Ltd.

Substantially Equivalent

510(k) numberK223492

Submission

Device name
eFOLDi Scooter, Lite
Applicant
Suntech UK , Ltd.
Rehill, GB
Received
November 21, 2022
Decision date
February 22, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
INI – Vehicle, Motorized 3-Wheeled
Device class
Class II (moderate risk)
Regulation
21 CFR 890.3800
Specialty
Physical Medicine

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Questions and answers

When was eFOLDi Scooter, Lite cleared by the FDA?

eFOLDi Scooter, Lite (K223492) received a 510(k) decision of Substantially Equivalent on February 22, 2023, 93 days after the submission was received.

What is the product code of K223492?

The FDA product code is INI – Vehicle, Motorized 3-Wheeled, a Class II (moderate risk) device regulated under 21 CFR 890.3800.