Battery Powered Patient Lift

FDA 510(k) K840997 · Invacare Corp.

Substantially Equivalent

510(k) numberK840997

Submission

Device name
Battery Powered Patient Lift
Applicant
Invacare Corp.
Elyria, OH, US
Received
March 8, 1984
Decision date
April 17, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FSA – Lift, Patient, Non-Ac-Powered
Device class
Class I (low risk)
Regulation
21 CFR 880.5510
Specialty
General Hospital

Other 510(k)s with product code FSA

510(k)DeviceApplicantDecision
K942807Surgical Lift SheetFSA · Traditional Surgin Surgical Instrumentation, Inc.08/02/1994SE
K930625Sanitas Patient LiftFSA · Traditional Dutton-Lainson Co.09/13/1993SE
K902141Anolift - Portable & Anolift - GantryFSA · Traditional Anodyne Corp.09/12/1990SE
K860837Hoyer One-Touch Power LifterFSA · Traditional Ted Hoyer & Co., Inc.03/27/1986SE
K851844MoliftFSA · Traditional Madshus A/S05/17/1985SE
K844976Medi-Man Water Powered Bath Lift & Hydraulic LiftFSA · Traditional Medi-Man Rehabilitation Products, Inc.04/01/1985SE
K841398Variable Height Transfer ChairFSA · Traditional Setma, Inc.05/07/1984SE
K841395Shower TrolleyFSA · Traditional Setma, Inc.05/07/1984SE
K823206Martin Pelvic LiftFSA · Traditional Martin Pelvic Lift Co.04/28/1983SE
K811899Century Lift Transfer SystemFSA · Traditional Century Manufacturing Co.07/23/1981SE

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Questions and answers

When was Battery Powered Patient Lift cleared by the FDA?

Battery Powered Patient Lift (K840997) received a 510(k) decision of Substantially Equivalent on April 17, 1984, 40 days after the submission was received.

What is the product code of K840997?

The FDA product code is FSA – Lift, Patient, Non-Ac-Powered, a Class I (low risk) device regulated under 21 CFR 880.5510.