510(k) K973572

KELOCOTE SCAR GEL AND KELOCOTE LASER GEL by Hanson Medical, Inc. — Product Code MDA

K973572 is an FDA 510(k) premarket notification submitted by Hanson Medical, Inc. for the device "KELOCOTE SCAR GEL AND KELOCOTE LASER GEL". The FDA issued a decision of Substantially Equivalent on October 21, 1997. The device falls under product code MDA (Elastomer, Silicone, For Scar Management), a Class I device regulated under 21 CFR 878.4025. Hanson Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 21, 1997
Date Received
September 19, 1997
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