FDA 510(k) Application Details - K003948

Device Classification Name	Elastomer, Silicone, For Scar Management   More FDA Info for this Device
510(K) Number	K003948
Device Name	Elastomer, Silicone, For Scar Management
Applicant	BIODERMIS CORP. 3078 EAST SUNSET RD. SUITE #1 LAS VEGAS, NV 89120 US Other 510(k) Applications for this Company
Contact	JEFF S SCHLEUING Other 510(k) Applications for this Contact
Regulation Number	878.4025   More FDA Info for this Regulation Number
Classification Product Code	MDA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/21/2000
Decision Date	01/29/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review