MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT— 510(k) K844976

Name: FDA 510(k) clearance K844976
Creator: U.S. Food and Drug Administration
Published: 1985-04-01

Substantially Equivalent

Medi-Man Rehabilitation Products, Inc.

FDA 510(k) clearance K844976 for MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT, Substantially Equivalent on 1985-04-01. Applicant: Medi-Man Rehabilitation Products, Inc.. Device class: 1.

Clearance details

Applicant: Medi-Man Rehabilitation Products, Inc.
Product code: Code FSA
Device class: Class 1
Regulation: 21 CFR 880.5510
Advisory panel: General Hospital
Date received: 1984-12-26
Decision date: 1985-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mississauga, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code FSA

view all

K942807 — SURGICAL LIFT SHEET1994-08-02
K930625 — SANITAS PATIENT LIFT1993-09-13
K902141 — ANOLIFT - PORTABLE & ANOLIFT - GANTRY1990-09-12
K860837 — HOYER ONE-TOUCH POWER LIFTER1986-03-27
K851844 — MOLIFT1985-05-17

More clearances from Medi-Man Rehabilitation Products, Inc.

view all

K992779 — A-2000 BATHING SYSTEMS; HYDROSONIC BATHIN SYSTEM2000-01-13
K925195 — MALIBU BATHING SYSTEM1994-10-17
K924905 — MEDI-PLINTH1993-02-16

Adverse events under product code FSA

product code FSA

Death: 101
Injury: 767
Malfunction: 1,173
Other: 1
Total: 2,042

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.