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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Snare, Flexible
510(k) Number K943935
Device Name GIP/MEDI-GLOBE POLYPECTOMY SNARES
Applicant
MEDI-GLOBE CORP.
6202 SOUTH MAPLE AVE. # 131
TEMPE,  AZ  85283
Applicant Contact GINA M GALLEGOS
Correspondent
MEDI-GLOBE CORP.
6202 SOUTH MAPLE AVE. # 131
TEMPE,  AZ  85283
Correspondent Contact GINA M GALLEGOS
Regulation Number876.4300
Classification Product Code
FDI  
Date Received08/12/1994
Decision Date 05/26/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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