510(k) K010245

ACTIVHEAL SCAR MANAGEMENT DRESSING by Advanced Medical Solutions, Ltd. — Product Code MDA

K010245 is an FDA 510(k) premarket notification submitted by Advanced Medical Solutions, Ltd. for the device "ACTIVHEAL SCAR MANAGEMENT DRESSING". The FDA issued a decision of Substantially Equivalent on April 25, 2001. The device falls under product code MDA (Elastomer, Silicone, For Scar Management), a Class I device regulated under 21 CFR 878.4025. Advanced Medical Solutions, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 25, 2001
Date Received
January 25, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Elastomer, Silicone, For Scar Management
Device Class
Class I
Regulation Number
878.4025
Review Panel
SU
Submission Type