FDA 510(k) Application Details - K180660

Device Classification Name	Tomography, Optical Coherence   More FDA Info for this Device
510(K) Number	K180660
Device Name	Tomography, Optical Coherence
Applicant	Optovue, Inc. 2800 Bayview Drive Fremont, CA 94538 US Other 510(k) Applications for this Company
Contact	Indu Lakshman Other 510(k) Applications for this Contact
Regulation Number	886.1570   More FDA Info for this Regulation Number
Classification Product Code	OBO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/14/2018
Decision Date	06/08/2018
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