FDA 510(k) Application Details - K960500

Device Classification Name	Protector, Hearing (Insert)   More FDA Info for this Device
510(K) Number	K960500
Device Name	Protector, Hearing (Insert)
Applicant	VIRTUAL CORP. 521 S.W. 11TH SUITE 400 PORTLAND, OR 97205 US Other 510(k) Applications for this Company
Contact	JONATHAN D BIRCK Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	EWD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/02/1996
Decision Date	04/03/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review