PMA
P880087: KELMAN MULTIFLEX 2 MODELS: MT3-MT7 & MT2U-MT7U
FDA PMA · Intraocular lens · Alcon Laboratories
Key facts
| PMA number | P880087 |
|---|---|
| Trade name | KELMAN MULTIFLEX 2 MODELS: MT3-MT7 & MT2U-MT7U |
| Generic name | Intraocular lens |
| Applicant | Alcon Laboratories |
| Owner/operator | Alcon Laboratories, Inc. |
| Product code | HQL |
| Approval date | Jan 31, 1990 |
| Docket number | 90M-0054 |
| Notice date | Feb 27, 1990 |
| Establishment registration | 1610287 |
| FEI number | 1610287 |
At a glance
- 10–99 Supplements
- Jun 20, 2024 Latest supplement decision
- No Withdrawn
- No Summary of safety and effectiveness on file
- 100–999 UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: