ASCENDA— 510(k) K941642

Name: FDA 510(k) clearance K941642
Creator: U.S. Food and Drug Administration
Published: 1994-06-13

Substantially Equivalent

American Stair-Glide Corp.

FDA 510(k) clearance K941642 for ASCENDA, Substantially Equivalent on 1994-06-13. Applicant: American Stair-Glide Corp.. Device class: 2.

Clearance details

Applicant: American Stair-Glide Corp.
Product code: Code ING
Device class: Class 2
Regulation: 21 CFR 890.3930
Advisory panel: Physical Medicine
Date received: 1994-04-04
Decision date: 1994-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grandview, MO, US

Download summary PDF View on FDA.gov ↗

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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.