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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Tubing, Noninvasive
510(k) Number K840838
Device Name MMG CONNECTIVE TUBING
Applicant
MEDICAL MARKETING GROUP
5335 DIVIDEND DR.
DECATUR,  GA  30035
Applicant Contact TIMOTHY D GOLDEN
Correspondent
MEDICAL MARKETING GROUP
5335 DIVIDEND DR.
DECATUR,  GA  30035
Correspondent Contact TIMOTHY D GOLDEN
Regulation Number880.6740
Classification Product Code
GAZ  
Date Received02/24/1984
Decision Date 03/30/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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