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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Mask, Surgical
510(k) Number K884392
Device Name KBM DENTAL MASK
Applicant
Kawamoto Bandage Material Co., Ltd.
4-1 Itoyamachi 2-Chome Chuoku
Osaka,  JP 540
Applicant Contact KAWAMOTO
Correspondent
Kawamoto Bandage Material Co., Ltd.
4-1 Itoyamachi 2-Chome Chuoku
Osaka,  JP 540
Correspondent Contact KAWAMOTO
Regulation Number878.4040
Classification Product Code
FXX  
Date Received10/18/1988
Decision Date 11/18/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
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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