FDA 510(k) Application Details - K182942

Device Classification Name	Tomography, Optical Coherence   More FDA Info for this Device
510(K) Number	K182942
Device Name	Tomography, Optical Coherence
Applicant	Canon Inc. 9-1, Imaikami-cho Nakahara-ku, Kawasaki 211-08501 JP Other 510(k) Applications for this Company
Contact	Tatsuya Yamazaki 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	10/23/2018
Decision Date	07/24/2019
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