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Acuity 181™ (tisilfocon A) and Acuity 181™ (tisilfocon A) with Tangible™ Hydra-PEG® Rigid Gas Permeable Contact Lenses

K242393 Class II Traditional
Decision Date
2024-11-01
Sponsor / Applicant
Acuity Polymers, Inc.

Technical Specification

510(k) Submission ID K242393
Product Code HQD
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5916
Decision Date 2024-11-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Acuity 181™ (tisilfocon A) and Acuity 181™ (tisilfocon A) with Tangible™ Hydra-PEG® Rigid Gas Permeable Contact Lenses received FDA 510(k) clearance under submission number K242393, sponsored by Acuity Polymers, 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 2024-11-01.

Classification & Regulation

This clearance is catalogued under FDA product code HQD and 21 CFR 886.5916, within the Ophthalmic review panel as a Class II device.