meddevicedb.com FDA Device Reference

Aqua Naina Sterile Saline Solution

K193441 Class II Traditional
Decision Date
2020-05-26
Sponsor / Applicant
Chemtex USA, Inc.

Technical Specification

510(k) Submission ID K193441
Product Code LPN
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5928
Decision Date 2020-05-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Aqua Naina Sterile Saline Solution received FDA 510(k) clearance under submission number K193441, sponsored by Chemtex USA, 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 2020-05-26.

Classification & Regulation

This clearance is catalogued under FDA product code LPN and 21 CFR 886.5928, within the Ophthalmic review panel as a Class II device.