510(k) K944581

CUTINOVA THIN WOUND DRESSING by Beiersdorf, Inc. — Product Code KMF

K944581 is an FDA 510(k) premarket notification submitted by Beiersdorf, Inc. for the device "CUTINOVA THIN WOUND DRESSING". The FDA issued a decision of SN on December 2, 1994. The device falls under product code KMF (Bandage, Liquid), a Class I device regulated under 21 CFR 880.5090. Beiersdorf, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
December 2, 1994
Date Received
September 19, 1994
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