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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 K945062
Device Name VACPLUS
Applicant
KINETIC CONCEPTS, INC.
P.O. BOX 659508
SAN ANTONIO,  TX  78265 -9508
Applicant Contact WILLIAM H QUIRK
Correspondent
KINETIC CONCEPTS, INC.
P.O. BOX 659508
SAN ANTONIO,  TX  78265 -9508
Correspondent Contact WILLIAM H QUIRK
Regulation Number878.4780
Classification Product Code
JCX  
Date Received10/14/1994
Decision Date 03/14/1995
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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