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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Bedding, Disposable, Medical
510(k) Number K870522
Device Name DEPEND UNDERPAD
Applicant
KIMBERLY-CLARK CORP.
1201 PENNSYLVANIA AVENUE, N.W.
SUITE 730
WASHINGTON,  DC  20004
Applicant Contact BONNIE B WAN
Correspondent
KIMBERLY-CLARK CORP.
1201 PENNSYLVANIA AVENUE, N.W.
SUITE 730
WASHINGTON,  DC  20004
Correspondent Contact BONNIE B WAN
Regulation Number880.6060
Classification Product Code
KME  
Date Received02/06/1987
Decision Date 03/13/1987
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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