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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 K951906
Device Name CARDON PHYSICAL THERAPY TABLES MODELS R28591 & R28592
Applicant
Cardon Rehabilitation Products, Inc.
16617 Killdeer Dr.
Rockville,  MD  20855
Applicant Contact GLENN E CONKLIN
Correspondent
Cardon Rehabilitation Products, Inc.
16617 Killdeer Dr.
Rockville,  MD  20855
Correspondent Contact GLENN E CONKLIN
Regulation Number890.3760
Classification Product Code
INQ  
Date Received04/24/1995
Decision Date 06/15/1995
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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