Avanticare, Model SA4022

FDA 510(k) K051538 · Lerado China Limited

Substantially Equivalent

510(k) numberK051538

Submission

Device name
Avanticare, Model SA4022
Applicant
Lerado China Limited
Taichung, TW
Received
June 10, 2005
Decision date
July 21, 2005
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 Avanticare, Model SA4022 cleared by the FDA?

Avanticare, Model SA4022 (K051538) received a 510(k) decision of Substantially Equivalent on July 21, 2005, 41 days after the submission was received.

What is the product code of K051538?

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