PMA supplement
P060022 S021: AKREOS INTRAOCULAR LENS
FDA PMA supplement · 30-Day Notice · Bausch & Lomb, Inc.
Key facts
| Original PMA | P060022 |
|---|---|
| Supplement number | S021 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | AKREOS INTRAOCULAR LENS |
| Generic name | Intraocular lens |
| Applicant | Bausch & Lomb, Inc. |
| Product code | HQL |
| Received date | Feb 18, 2015 |
| Decision date | Mar 20, 2015 |
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: