PATIENT SUPPORT SYSTEM— 510(k) K940872

Name: FDA 510(k) clearance K940872
Creator: U.S. Food and Drug Administration
Published: 1994-10-13

Substantially Equivalent

Arylift, Inc.

FDA 510(k) clearance K940872 for PATIENT SUPPORT SYSTEM, Substantially Equivalent on 1994-10-13. Applicant: Arylift, Inc.. Device class: 2.

Clearance details

Applicant: Arylift, Inc.
Product code: Code FNG
Device class: Class 2
Regulation: 21 CFR 880.5500
Advisory panel: General Hospital
Date received: 1994-02-25
Decision date: 1994-10-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FNG

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K121287 — HT-WEDGE2012-10-03
K041503 — HOVERJACK AIR PATIENT LIFT DEVICE2004-08-12
K935351 — A.C. POWER PATIENT LIFT1994-02-28
K926411 — SAF-LIFT/SAF-KARY1993-03-31
K912769 — PATIENT LIFT AND TRANSPORT1991-10-02

Adverse events under product code FNG

product code FNG

Death: 4
Total: 4

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.