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EXTREME H20 (HIOXIFILICON A) SOFT CONTACT LENS

K992692 Class II Traditional
Decision Date
1999-10-18
Sponsor / Applicant
Benz Research and Development Corp.

Technical Specification

510(k) Submission ID K992692
Product Code LPL
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5925
Decision Date 1999-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXTREME H20 (HIOXIFILICON A) SOFT CONTACT LENS received FDA 510(k) clearance under submission number K992692, sponsored by Benz Research and Development Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1999-10-18.

Classification & Regulation

This clearance is catalogued under FDA product code LPL and 21 CFR 886.5925, within the Ophthalmic review panel as a Class II device.