PMA
P880090: MODEL 120UV ANTERIOR CHAMBER INTRAOCULAR LENS
FDA PMA · Intraocular lens · Bausch & Lomb, Inc.
Key facts
| PMA number | P880090 |
|---|---|
| Trade name | MODEL 120UV ANTERIOR CHAMBER INTRAOCULAR LENS |
| Generic name | Intraocular lens |
| Applicant | Bausch & Lomb, Inc. |
| Owner/operator | Bausch & Lomb Incorporated |
| Product code | HQL |
| Approval date | Dec 28, 1989 |
| Docket number | 90M-0005 |
| Notice date | Jan 30, 1990 |
| Establishment registration | 1281950 |
| FEI number | 1281950 |
At a glance
- 10–99 Supplements
- Feb 28, 2019 Latest supplement decision
- No Withdrawn
- No Summary of safety and effectiveness on file
- 1–9 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: