PMA supplement
P180035 S002: MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Daily Wear Contact Lenses
FDA PMA supplement · 30-Day Notice · CooperVision, Inc.
Key facts
| Original PMA | P180035 |
|---|---|
| Supplement number | S002 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Daily Wear Contact Lenses |
| Generic name | Daily wear soft contact lens to reduce the progression of myopia |
| Applicant | CooperVision, Inc. |
| Product code | QIT |
| Received date | Jan 9, 2020 |
| Decision date | Feb 4, 2020 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: