FDA 510(k) Application Details - K221320

Device Classification Name	Tomography, Optical Coherence   More FDA Info for this Device
510(K) Number	K221320
Device Name	Tomography, Optical Coherence
Applicant	Nidek Co., LTD. 34-14 Maehama, Hiroishi-cho Gamagori 443-0038 JP Other 510(k) Applications for this Company
Contact	Tsutomu Sunada 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	05/06/2022
Decision Date	03/30/2023
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