SAF-LIFT/SAF-KARY— 510(k) K926411

Name: FDA 510(k) clearance K926411
Creator: U.S. Food and Drug Administration
Published: 1993-03-31

Substantially Equivalent

Arjo-Century, Inc.

FDA 510(k) clearance K926411 for SAF-LIFT/SAF-KARY, Substantially Equivalent on 1993-03-31. Applicant: Arjo-Century, Inc.. Device class: 2.

Clearance details

Applicant: Arjo-Century, Inc.
Product code: Code FNG
Device class: Class 2
Regulation: 21 CFR 880.5500
Advisory panel: General Hospital
Date received: 1992-12-21
Decision date: 1993-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Aurora, NE, 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
K912769 — PATIENT LIFT AND TRANSPORT1991-10-02

More clearances from Arjo-Century, Inc.

view all

K930665 — CENTURY BATHING SYSTEM1995-08-28
K923637 — ARJO-CENTURY ARM AND LEG TANK SYSTEM1993-02-12
K923617 — FULL MOVEMENT THERAPY SYSTEMS1992-11-09
K923159 — ARJO-CENTURY PODIATRIC WHIRLPOOL SYSTEMS1992-08-06
K920074 — ARJO CENTURY SCALES WITH REMOTE1992-04-06

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.