FDA product code QIT: Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia
QIT is the FDA product code for daily wear soft contact lens to reduce the progression of myopia. It is a Class III device, reviewed by the Ophthalmic panel. Devices under QIT reach the market by PMA; FDA lists no cleared 510(k)s for it. 1 PMA application cites this product code.
Definition
Intended to be worn on the surface of the eye in children who have myopia to: Reduce the rate of progression of myopia, and Optically correct myopic refractive error.
Classification
| Field | Value |
|---|---|
| Device name | Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia |
| Device class | Class III |
| Review panel | OP — Ophthalmic |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for QIT devices
openFDA lists no recalls for product code QIT.
Frequently asked questions
What is FDA product code QIT?
QIT is the FDA product code for daily wear soft contact lens to reduce the progression of myopia. It is a Class III device, reviewed by the Ophthalmic panel.
What device class is QIT?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code QIT
- Run a recall and safety report across every QIT manufacturer
- Watch product code QIT for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.