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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Alarm, Conditioned Response Enuresis
510(k) Number K901906
Device Name WET-NO-MORE MONITOR
Applicant
Travis Industries, Inc.
100 Main-Sumner
Coos Bay,  OR  97420
Correspondent
Travis Industries, Inc.
100 Main-Sumner
Coos Bay,  OR  97420
Regulation Number876.2040
Classification Product Code
KPN  
Date Received04/27/1990
Decision Date 07/11/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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