KYMCO EQ10D Scooter— 510(k) K163201

Name: FDA 510(k) clearance K163201
Creator: U.S. Food and Drug Administration
Published: 2017-03-16

Substantially Equivalent

Kwang Yang Motor Co., Ltd.

FDA 510(k) clearance K163201 for KYMCO EQ10D Scooter, Substantially Equivalent on 2017-03-16. Applicant: Kwang Yang Motor Co., Ltd.. Device class: 2.

Clearance details

Applicant: Kwang Yang Motor Co., Ltd.
Product code: Code INI
Device class: Class 2
Regulation: 21 CFR 890.3800
Advisory panel: Physical Medicine
Date received: 2016-11-15
Decision date: 2017-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kaohsiung, TW

Download summary PDF View on FDA.gov ↗

Recent devices under product code INI

view all

K260094 — Mobility Scooter (W3465, W3902 (S50 Carbon))2026-08-10
K260176 — Mobility Scooter (W3483, W3483A)2026-08-10
K261232 — IERO Mobility Scooter (IERO-01)2026-07-14
K261163 — Mobility Scooter (R200)2026-07-07
K253257 — Virgo Mobility Scooter (Virgo-D,Virgo-F)2026-06-08

More clearances from Kwang Yang Motor Co., Ltd.

view all

K130940 — KYMCO EQ20C SCOOTER2013-10-07
K082900 — KYMCO FORU, MODEL EQ102008-10-28
K082901 — KYMCO FORU, MODEL EQ202008-10-28
K081133 — KYMCO FORU, MODEL EQ402008-06-10
K072630 — FORU, MODEL EQ302007-10-03

Adverse events under product code INI

product code INI

Injury: 171
Other: 1
Total: 172

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.