510(k) K952526

CUTINOVA CAVITY by Beiersdorf, Inc. — Product Code KMF

Clearance Details

Decision
SN ()
Decision Date
August 14, 1995
Date Received
June 1, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bandage, Liquid
Device Class
Class I
Regulation Number
880.5090
Review Panel
SU
Submission Type