510(k) K921760

TRICOPLAST by Beiersdorf, Inc. — Product Code KGX

K921760 is an FDA 510(k) premarket notification submitted by Beiersdorf, Inc. for the device "TRICOPLAST". The FDA issued a decision of Substantially Equivalent on August 10, 1992. 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
August 10, 1992
Date Received
April 14, 1992
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