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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 K925563
Device Name FT MODEL TABLE W/ELECTRIC HI LO OPTION E
Applicant
Pro Med Mfg., Inc.
10750 Mankato St.
Blaine,  MN  55449
Applicant Contact KIRSTEN BOVY
Correspondent
Pro Med Mfg., Inc.
10750 Mankato St.
Blaine,  MN  55449
Correspondent Contact KIRSTEN BOVY
Regulation Number890.3760
Classification Product Code
INQ  
Date Received11/03/1992
Decision Date 05/26/1993
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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