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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Lift, Patient, Non-Ac-Powered
510(k) Number K844976
Device Name MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT
Applicant
Medi-Man Rehabilitation Products, Inc.
1020 Meyerside Dr., Unit #1
Mississauga,  CA
Applicant Contact GORDAN CLARD
Correspondent
Medi-Man Rehabilitation Products, Inc.
1020 Meyerside Dr., Unit #1
Mississauga,  CA
Correspondent Contact GORDAN CLARD
Regulation Number880.5510
Classification Product Code
FSA  
Date Received12/26/1984
Decision Date 04/01/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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