SUPERARM 2000 LIFT— 510(k) K901381

Substantially Equivalent

Handicaps, Inc.

FDA 510(k) clearance K901381 for SUPERARM 2000 LIFT, Substantially Equivalent on 1990-04-16. Applicant: Handicaps, Inc..

Clearance details

Applicant: Handicaps, Inc.
Product code: Code ING
Advisory panel: Physical Medicine
Date received: 1990-03-22
Decision date: 1990-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Englewood, CO, US

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Adverse events under product code ING

product code ING

Death: 3
Total: 3

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.