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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name clamp, surgical, general & plastic surgery
510(k) Number K924223
Device Name MAR-MED LIVER STRAP
Applicant
MAR-MED CO.
353 FULLER N.E.
GRAND RAPIDS,  MI  49503
Applicant Contact JOSEPH B MAROGIL
Correspondent
MAR-MED CO.
353 FULLER N.E.
GRAND RAPIDS,  MI  49503
Correspondent Contact JOSEPH B MAROGIL
Regulation Number878.4800
Classification Product Code
GDJ  
Date Received08/21/1992
Decision Date 03/18/1993
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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