FDA 510(k) Application Details - K133892

Device Classification Name	Ophthalmoscope, Ac-Powered   More FDA Info for this Device
510(K) Number	K133892
Device Name	Ophthalmoscope, Ac-Powered
Applicant	OPTOVUE, INC. 2800 BAYVIEW DRIVE FREMONT, CA 94538 US Other 510(k) Applications for this Company
Contact	MICHAEL J SARRASIN Other 510(k) Applications for this Contact
Regulation Number	886.1570   More FDA Info for this Regulation Number
Classification Product Code	HLI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/20/2013
Decision Date	03/19/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review