SUPERARM 2000 LIFT— 510(k) K901381

Name: FDA 510(k) clearance K901381
Creator: U.S. Food and Drug Administration
Published: 1990-04-16

Substantially Equivalent

Handicaps, Inc.

FDA 510(k) clearance K901381 for SUPERARM 2000 LIFT, Substantially Equivalent on 1990-04-16. Applicant: Handicaps, Inc.. Device class: 2.

Clearance details

Applicant: Handicaps, Inc.
Product code: Code ING
Device class: Class 2
Regulation: 21 CFR 890.3930
Advisory panel: Physical Medicine
Date received: 1990-03-22
Decision date: 1990-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Englewood, CO, US

Download summary PDF View on FDA.gov ↗

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K091881 — RPL/CPL VERTICAL PLATFORM LIFTS2009-07-01
K090856 — JOURNEY (OR RPSP), JOURNEY CUBIC (OR SUPRA OR TP02)2009-05-27

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.