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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name table, surgical with orthopedic accessories, ac-powered
510(k) Number K894789
Device Name DMI 250 SERIES POWER SURGERY TABLE
Applicant
M.D. INTL., INC.
2601 SOUTH 2700 WEST
SALT LAKE CITY,  UT  84119
Applicant Contact JOHANNE D YOUNG
Correspondent
M.D. INTL., INC.
2601 SOUTH 2700 WEST
SALT LAKE CITY,  UT  84119
Correspondent Contact JOHANNE D YOUNG
Regulation Number878.4960
Classification Product Code
JEA  
Date Received07/28/1989
Decision Date 08/29/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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