510(k) K935803

CICA-CARE SILICONE GEL SHEET by Smith & Nephew United, Inc. — Product Code MDA

K935803 is an FDA 510(k) premarket notification submitted by Smith & Nephew United, Inc. for the device "CICA-CARE SILICONE GEL SHEET". The FDA issued a decision of Substantially Equivalent on February 3, 1994. The device falls under product code MDA (Elastomer, Silicone, For Scar Management), a Class I device regulated under 21 CFR 878.4025. Smith & Nephew United, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 3, 1994
Date Received
December 2, 1993
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