COACH 888— 510(k) K030758

Name: FDA 510(k) clearance K030758
Creator: U.S. Food and Drug Administration
Published: 2003-07-31

Substantially Equivalent

Wheelchair & Scooter Express

FDA 510(k) clearance K030758 for COACH 888, Substantially Equivalent on 2003-07-31. Applicant: Wheelchair & Scooter Express. Device class: 2.

Clearance details

Applicant: Wheelchair & Scooter Express
Product code: Code INI
Device class: Class 2
Regulation: 21 CFR 890.3800
Advisory panel: Physical Medicine
Date received: 2003-03-11
Decision date: 2003-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code INI

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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 Wheelchair & Scooter Express

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K030756 — COACH 777-32003-10-06
K030757 — COACH 777-42003-10-06
K032441 — F-10 FOLDING POWER CHAIR2003-10-06
K032440 — F-11 FOLDING POWER CHAIR2003-09-23
K030760 — COACH 888W2003-07-10

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.