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METRO FOCAL ASPHERIC (POLYMACON)

K961606 Class II Traditional
Decision Date
1996-11-20
Sponsor / Applicant
Metro Optics of Austin, Inc.

Technical Specification

510(k) Submission ID K961606
Product Code LPL
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5925
Decision Date 1996-11-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

METRO FOCAL ASPHERIC (POLYMACON) received FDA 510(k) clearance under submission number K961606, sponsored by Metro Optics of Austin, 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 1996-11-20.

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.