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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Strip, Adhesive, Closure, Skin
510(k) Number K792725
Device Name FIXOMULL
Applicant
BEIERSDORF, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
BEIERSDORF, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number880.5240
Classification Product Code
FPX  
Date Received12/31/1979
Decision Date 03/05/1980
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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