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RENU MULTIPLUS MULTI-PURPOSE DISINFECTING SOLUTION

K002823 Class II Traditional
Decision Date
2000-10-17
Sponsor / Applicant
Bausch & Lomb, Inc.

Technical Specification

510(k) Submission ID K002823
Product Code LPN
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5928
Decision Date 2000-10-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RENU MULTIPLUS MULTI-PURPOSE DISINFECTING SOLUTION received FDA 510(k) clearance under submission number K002823, sponsored by Bausch & Lomb, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2000-10-17.

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.