PMA
P850033: SCANLENS (SCAFILCON A CONTACT LENS)
FDA PMA · Lenses, soft contact, daily wear · Ciba Vision Corporation
Key facts
| PMA number | P850033 |
|---|---|
| Trade name | SCANLENS (SCAFILCON A CONTACT LENS) |
| Generic name | Lenses, soft contact, daily wear |
| Applicant | Ciba Vision Corporation |
| Owner/operator | Alcon Laboratories, Inc. |
| Product code | LPL |
| Approval date | Nov 28, 1986 |
| Docket number | 86M-0501 |
| Notice date | Jan 16, 1987 |
| Establishment registration | 9610813 |
| FEI number | 1000115040 |
At a glance
- 1–9 Supplements
- Jul 28, 1988 Latest supplement decision
- Yes Withdrawn
- No Summary of safety and effectiveness on file
- None 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: