MICROLITE WHEELCHAIR— 510(k) K933919

Name: FDA 510(k) clearance K933919
Creator: U.S. Food and Drug Administration
Published: 1993-09-30

Substantially Equivalent

Morgan Technology, Inc.

FDA 510(k) clearance K933919 for MICROLITE WHEELCHAIR, Substantially Equivalent on 1993-09-30. Applicant: Morgan Technology, Inc.. Device class: 1.

Clearance details

Applicant: Morgan Technology, Inc.
Product code: Code IOR
Device class: Class 1
Regulation: 21 CFR 890.3850
Advisory panel: Physical Medicine
Date received: 1993-08-10
Decision date: 1993-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Downers Grove, IL, US

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Adverse events under product code IOR

product code IOR

Death: 10
Injury: 232
Other: 2
Total: 244

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.