510(k) K896891

LEUKOSILK(TM) SURGICAL TAPE by Beiersdorf, Inc. — Product Code KGX

K896891 is an FDA 510(k) premarket notification submitted by Beiersdorf, Inc. for the device "LEUKOSILK(TM) SURGICAL TAPE". The FDA issued a decision of Substantially Equivalent on February 9, 1990. The device falls under product code KGX (Tape And Bandage, Adhesive), a Class I device regulated under 21 CFR 880.5240. Beiersdorf, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 9, 1990
Date Received
December 8, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tape And Bandage, Adhesive
Device Class
Class I
Regulation Number
880.5240
Review Panel
SU
Submission Type