RODEO MODEL, RD12, RD14, RD16, RADIO TRANSIT MODEL, RD12T, RD14T, RD16T,— 510(k) K032402

Name: FDA 510(k) clearance K032402
Creator: U.S. Food and Drug Administration
Published: 2003-09-24

Substantially Equivalent

Convaid Products, Inc.

FDA 510(k) clearance K032402 for RODEO MODEL, RD12, RD14, RD16, RADIO TRANSIT MODEL, RD12T, RD14T, RD16T,, Substantially Equivalent on 2003-09-24. Applicant: Convaid Products, Inc.. Device class: 1.

Clearance details

Applicant: Convaid Products, Inc.
Product code: Code IOR
Device class: Class 1
Regulation: 21 CFR 890.3850
Advisory panel: Physical Medicine
Date received: 2003-08-04
Decision date: 2003-09-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Torrance, CA, US

Download summary PDF View on FDA.gov ↗

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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.