Aqua Naina Plus Sterile Saline Solution

FDA 510(k) K221263 · Chemtex USA, Inc.

Substantially Equivalent

510(k) numberK221263

Submission

Device name
Aqua Naina Plus Sterile Saline Solution
Applicant
Chemtex USA, Inc.
Fairfield, NJ, US
Received
May 2, 2022
Decision date
October 12, 2022
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LPN – Accessories, Soft Lens Products
Device class
Class II (moderate risk)
Regulation
21 CFR 886.5928
Specialty
Ophthalmic

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Questions and answers

When was Aqua Naina Plus Sterile Saline Solution cleared by the FDA?

Aqua Naina Plus Sterile Saline Solution (K221263) received a 510(k) decision of Substantially Equivalent on October 12, 2022, 163 days after the submission was received.

What is the product code of K221263?

The FDA product code is LPN – Accessories, Soft Lens Products, a Class II (moderate risk) device regulated under 21 CFR 886.5928.