FDA 510(k) Application Details - K210701

Device Classification Name	Ophthalmic Femtosecond Laser   More FDA Info for this Device
510(K) Number	K210701
Device Name	Ophthalmic Femtosecond Laser
Applicant	AMO Manufacturing USA, LLC 510 Cottonwood Drive Milpitas, CA 95035 US Other 510(k) Applications for this Company
Contact	Laarni Ricafort Other 510(k) Applications for this Contact
Regulation Number	886.4390   More FDA Info for this Regulation Number
Classification Product Code	OOE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/09/2021
Decision Date	04/07/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review