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METRO 55G TORIC & SPHERICAL

K953199 Class II Traditional
Decision Date
1995-12-11
Sponsor / Applicant
Metrosoft, Inc.

Technical Specification

510(k) Submission ID K953199
Product Code LPL
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5925
Decision Date 1995-12-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

METRO 55G TORIC & SPHERICAL received FDA 510(k) clearance under submission number K953199, sponsored by Metrosoft, 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 1995-12-11.

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.