FDA 510(k) Application Details - K153181

Device Classification Name	Ophthalmoscope,Laser,Scanning   More FDA Info for this Device
510(K) Number	K153181
Device Name	Ophthalmoscope,Laser,Scanning
Applicant	CENTERVUE SPA VIA SAN MARCO 9H PADOVA 35129 IT Other 510(k) Applications for this Company
Contact	ROBERTO GABRIOTTI Other 510(k) Applications for this Contact
Regulation Number	886.1570   More FDA Info for this Regulation Number
Classification Product Code	MYC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/03/2015
Decision Date	06/08/2016
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