FDA 510(k) Application Details - K202932

Device Classification Name	Accessories, Soft Lens Products   More FDA Info for this Device
510(K) Number	K202932
Device Name	Accessories, Soft Lens Products
Applicant	Bausch & Lomb Incorporated 1400 North Goodman Street Rochester, NY 14609 US Other 510(k) Applications for this Company
Contact	Melissa Thomas Other 510(k) Applications for this Contact
Regulation Number	886.5928   More FDA Info for this Regulation Number
Classification Product Code	LPN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/29/2020
Decision Date	05/28/2021
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