meddevicedb.com FDA Device Reference

Precision1; Precision1 for Astigmatism; Dailies Total1; Dailies Total1 for Astigmatism; Dailies Total1 Multifocal; Dailies Total1 Multifocal Toric

K243909 Class II Special
Decision Date
2025-01-13
Sponsor / Applicant
Alcon Laboratories, Inc.

Technical Specification

510(k) Submission ID K243909
Product Code LPL
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5925
Decision Date 2025-01-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Precision1; Precision1 for Astigmatism; Dailies Total1; Dailies Total1 for Astigmatism; Dailies Total1 Multifocal; Dailies Total1 Multifocal Toric received FDA 510(k) clearance under submission number K243909, sponsored by Alcon Laboratories, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2025-01-13.

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.