FDA 510(k) Application Details - K960404

Device Classification Name	Dressing, Wound And Burn, Occlusive   More FDA Info for this Device
510(K) Number	K960404
Device Name	Dressing, Wound And Burn, Occlusive
Applicant	EUROMED A/S 49 PLAIN ST. NORTH ATTLEBORO, MA 02760 US Other 510(k) Applications for this Company
Contact	DIANE E MINEAR Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MGP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/29/1996
Decision Date	03/01/1996
Decision	SN - Substantially Equivalent for Some Indications
Classification Advisory Committee	-
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type	Traditional
Reviewed By Third Party	N
Expedited Review