meddevicedb.com FDA Device Reference

SOLO-CARE PLUS MULTIPURPOSE SOLUTION

K012731 Class II Traditional
Decision Date
2001-12-26
Sponsor / Applicant
Ciba Vision Corporation

Technical Specification

510(k) Submission ID K012731
Product Code LPN
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5928
Decision Date 2001-12-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOLO-CARE PLUS MULTIPURPOSE SOLUTION received FDA 510(k) clearance under submission number K012731, sponsored by Ciba Vision Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2001-12-26.

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.