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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 K950873
Device Name CARDON PHYSICAL THERAPY TABLES MODELS: R27622
Applicant
Cardon Rehabilitation Products, Inc.
2045 Niagara Falls Blvd.,
Unit #5, P.O. Box 237
Niagara Falls,  NY  14304
Applicant Contact C. E CARDON
Correspondent
Cardon Rehabilitation Products, Inc.
2045 Niagara Falls Blvd.,
Unit #5, P.O. Box 237
Niagara Falls,  NY  14304
Correspondent Contact C. E CARDON
Regulation Number890.3760
Classification Product Code
INQ  
Date Received02/28/1995
Decision Date 04/10/1995
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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