meddevicedb.com FDA Device Reference

Bausch + Lomb Sensitive Eyes Plus Saline Solution

K170483 Class II Traditional
Decision Date
2017-04-11
Sponsor / Applicant
Bausch & Lomb, Incorporated

Technical Specification

510(k) Submission ID K170483
Product Code LPN
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5928
Decision Date 2017-04-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Bausch + Lomb Sensitive Eyes Plus Saline Solution received FDA 510(k) clearance under submission number K170483, sponsored by Bausch & Lomb, Incorporated. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2017-04-11.

Classification & Regulation

This clearance is catalogued under FDA product code LPN and 21 CFR 886.5928, within the Ophthalmic review panel as a Class II device.