PMA
P880029: B AND L 70 LIDOFILCON A CONTACT LENSE
FDA PMA · Lenses, soft contact, extended wear · Bausch & Lomb, Inc.
Key facts
| PMA number | P880029 |
|---|---|
| Trade name | B AND L 70 LIDOFILCON A CONTACT LENSE |
| Generic name | Lenses, soft contact, extended wear |
| Applicant | Bausch & Lomb, Inc. |
| Owner/operator | Bausch & Lomb Incorporated |
| Product code | LPM |
| Approval date | Apr 29, 1988 |
| Docket number | 88M-0188 |
| Notice date | Jul 19, 1988 |
| Establishment registration | 1313525 |
| FEI number | 1317628 |
At a glance
- 10–99 Supplements
- Jun 28, 2002 Latest supplement decision
- Yes Withdrawn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: