PMA
P790027: CHAMBER LENS MODELS 101, 101B, 101T
FDA PMA · Intraocular lens · Bausch & Lomb
Key facts
| PMA number | P790027 |
|---|---|
| Trade name | CHAMBER LENS MODELS 101, 101B, 101T |
| Generic name | Intraocular lens |
| Applicant | Bausch & Lomb |
| Owner/operator | Bausch & Lomb Incorporated |
| Product code | HQL |
| Approval date | Mar 2, 1982 |
| Notice date | Mar 26, 1982 |
| Establishment registration | 1313525 |
| FEI number | 1317628 |
At a glance
- 10–99 Supplements
- Aug 13, 2003 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- Yes Withdrawn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: