PMA supplement
P870024 S002: FLUOROPERM RGP CONTACT LENSES
FDA PMA supplement · Panel Track · CooperVision, Inc.
Key facts
| Original PMA | P870024 |
|---|---|
| Supplement number | S002 |
| Supplement type | Panel Track |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | FLUOROPERM RGP CONTACT LENSES |
| Generic name | Lens, contact (other material) - daily |
| Applicant | CooperVision, Inc. |
| Product code | HQD |
| Received date | Mar 9, 1988 |
| Decision date | May 31, 1988 |
| Docket number | 88M-0220 |
| Notice date | Jul 12, 1988 |
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: