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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Physical Therapy, Multi Function
510(k) Number K905756
Device Name TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE
Applicant
Titan Technology Intl., Inc.
1515 N. Warson Rd.
Suite 200
St. Louis,  MI  63182
Applicant Contact HOWARD COOPER
Correspondent
Titan Technology Intl., Inc.
1515 N. Warson Rd.
Suite 200
St. Louis,  MI  63182
Correspondent Contact HOWARD COOPER
Regulation Number890.5880
Classification Product Code
JFB  
Date Received12/27/1990
Decision Date 01/08/1991
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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