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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Powered
510(k) Number K924905
Device Name MEDI-PLINTH
Applicant
Medi-Man Rehabilitation Products, Inc.
5630 Tomken Rd.
Mississauga, Ontario,
Canada, L4w 1p4,  CA
Applicant Contact JANE BELROSE
Correspondent
Medi-Man Rehabilitation Products, Inc.
5630 Tomken Rd.
Mississauga, Ontario,
Canada, L4w 1p4,  CA
Correspondent Contact JANE BELROSE
Regulation Number890.3760
Classification Product Code
INQ  
Date Received09/29/1992
Decision Date 02/16/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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