510(k) K022645

CURAD by Beiersdorf AG — Product Code KMF

K022645 is an FDA 510(k) premarket notification submitted by Beiersdorf AG for the device "CURAD". The FDA issued a decision of Substantially Equivalent on November 5, 2002. The device falls under product code KMF (Bandage, Liquid), a Class I device regulated under 21 CFR 880.5090. Beiersdorf AG has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 5, 2002
Date Received
August 8, 2002
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