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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name apparatus, suction, ward use, portable, ac-powered
510(k) Number K843081
Device Name TUGS-TRANSPORTABLE UNIV. GRADIENT SUCT
Applicant
CREATIVE MEDICAL LABORATORIES, INC.
P.O. BOX 6347
Applicant Contact ALLEN W MOBERG
Correspondent
CREATIVE MEDICAL LABORATORIES, INC.
P.O. BOX 6347
Correspondent Contact ALLEN W MOBERG
Regulation Number878.4780
Classification Product Code
JCX  
Date Received08/06/1984
Decision Date 10/11/1984
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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