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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name table, operating-room, ac-powered
510(k) Number K926463
Device Name RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCES
Applicant
MIDMARK CORP.
60 VISTA DR.
P.O. BOX 286
VERSAILLES,  OH  45380
Applicant Contact BRADY K SEIDEN
Correspondent
MIDMARK CORP.
60 VISTA DR.
P.O. BOX 286
VERSAILLES,  OH  45380
Correspondent Contact BRADY K SEIDEN
Regulation Number878.4960
Classification Product Code
FQO  
Date Received12/24/1992
Decision Date 10/21/1994
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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