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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name tape and bandage, adhesive
510(k) Number K881397
Device Name SANAPLAST
Applicant
NEBO INDUSTRIES
P.O. BOX 241
FOUNTAIN GREEN,  UT  84632
Applicant Contact WARREN JACOBSON
Correspondent
NEBO INDUSTRIES
P.O. BOX 241
FOUNTAIN GREEN,  UT  84632
Correspondent Contact WARREN JACOBSON
Regulation Number880.5240
Classification Product Code
KGX  
Date Received04/04/1988
Decision Date 06/14/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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