meddevicedb.com FDA Device Reference

COMFEES(R) + CON-PAK(TM) LENS CASE

K897085 Class II Traditional
Decision Date
1990-02-28
Sponsor / Applicant
Magnivision, Inc.

Technical Specification

510(k) Submission ID K897085
Product Code LRX
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5928
Decision Date 1990-02-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMFEES(R) + CON-PAK(TM) LENS CASE received FDA 510(k) clearance under submission number K897085, sponsored by Magnivision, 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 1990-02-28.

Classification & Regulation

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