FDA 510(k) Application Details - K153769

Device Classification Name	Laser, Ophthalmic   More FDA Info for this Device
510(K) Number	K153769
Device Name	Laser, Ophthalmic
Applicant	Lutronic Corporation 219, Sowon-ro, Deogyang-gu Goyang-si 410-220 KR Other 510(k) Applications for this Company
Contact	Jhung Won Vojir Other 510(k) Applications for this Contact
Regulation Number	886.4390   More FDA Info for this Regulation Number
Classification Product Code	HQF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/30/2015
Decision Date	10/05/2016
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