Medi-Man Water Powered Bath Lift & Hydraulic Lift

FDA 510(k) K844976 · Medi-Man Rehabilitation Products, Inc.

Substantially Equivalent

510(k) numberK844976

Submission

Device name
Medi-Man Water Powered Bath Lift & Hydraulic Lift
Applicant
Medi-Man Rehabilitation Products, Inc.
Mississauga, CA
Received
December 26, 1984
Decision date
April 1, 1985
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
K841398Variable Height Transfer ChairFSA · Traditional Setma, Inc.05/07/1984SE
K841395Shower TrolleyFSA · Traditional Setma, Inc.05/07/1984SE
K840997Battery Powered Patient LiftFSA · Traditional Invacare Corp.04/17/1984SE
K823206Martin Pelvic LiftFSA · Traditional Martin Pelvic Lift Co.04/28/1983SE
K811899Century Lift Transfer SystemFSA · Traditional Century Manufacturing Co.07/23/1981SE

More from Century Manufacturing Co.

510(k)DeviceDecision
K992779A-2000 Bathing Systems; Hydrosonic Bathin SystemILJ · Traditional 01/13/2000SE
K925195Malibu Bathing SystemILJ · Traditional 10/17/1994SE
K924905Medi-PlinthINQ · Traditional 02/16/1993SE

Questions and answers

When was Medi-Man Water Powered Bath Lift & Hydraulic Lift cleared by the FDA?

Medi-Man Water Powered Bath Lift & Hydraulic Lift (K844976) received a 510(k) decision of Substantially Equivalent on April 1, 1985, 96 days after the submission was received.

What is the product code of K844976?

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