510(k) K963128

NOVAGEL SILICONE GEL SHEETING by Brennen Medical, Inc. — Product Code MDA

K963128 is an FDA 510(k) premarket notification submitted by Brennen Medical, Inc. for the device "NOVAGEL SILICONE GEL SHEETING". The FDA issued a decision of Substantially Equivalent on December 5, 1996. The device falls under product code MDA (Elastomer, Silicone, For Scar Management), a Class I device regulated under 21 CFR 878.4025. Brennen Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 5, 1996
Date Received
August 12, 1996
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