MURRAY CHAIR LIFT— 510(k) K854120

Name: FDA 510(k) clearance K854120
Creator: U.S. Food and Drug Administration
Published: 1985-11-01

Substantially Equivalent

J.B. Murray Enterprises, Inc.

FDA 510(k) clearance K854120 for MURRAY CHAIR LIFT, Substantially Equivalent on 1985-11-01. Applicant: J.B. Murray Enterprises, Inc.. Device class: 2.

Clearance details

Applicant: J.B. Murray Enterprises, Inc.
Product code: Code FNG
Device class: Class 2
Regulation: 21 CFR 880.5500
Advisory panel: General Hospital
Date received: 1985-10-09
Decision date: 1985-11-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bloomingdale, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FNG

view all

K121287 — HT-WEDGE2012-10-03
K041503 — HOVERJACK AIR PATIENT LIFT DEVICE2004-08-12
K940872 — PATIENT SUPPORT SYSTEM1994-10-13
K935351 — A.C. POWER PATIENT LIFT1994-02-28
K926411 — SAF-LIFT/SAF-KARY1993-03-31

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.