KARMA-RS, KARMA-FS WHEELCHAIRS— 510(k) K884812

Substantially Equivalent

Orthofab, Inc.

FDA 510(k) clearance K884812 for KARMA-RS, KARMA-FS WHEELCHAIRS, Substantially Equivalent on 1988-12-27. Applicant: Orthofab, Inc..

Clearance details

Applicant: Orthofab, Inc.
Product code: Code ITI
Advisory panel: Physical Medicine
Date received: 1988-11-17
Decision date: 1988-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canada, Gim 1c2, CA

Download summary PDF View on FDA.gov ↗

Adverse events under product code ITI

product code ITI

Death: 34
Injury: 778
Malfunction: 1,085
Other: 1
Total: 1,898

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.