FDA 510(k) Application Details - K220613

Device Classification Name	Lenses, Soft Contact, Daily Wear   More FDA Info for this Device
510(K) Number	K220613
Device Name	Lenses, Soft Contact, Daily Wear
Applicant	Bausch & Lomb Incorporated 1400 North Goodman street Rochester, NY 14609 US Other 510(k) Applications for this Company
Contact	Barbara Klube-Falso Other 510(k) Applications for this Contact
Regulation Number	886.5925   More FDA Info for this Regulation Number
Classification Product Code	LPL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/03/2022
Decision Date	03/08/2023
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