PMA
P960011: BIOLON 1% SODIUM HYALURONATE VISCOELASTIC SURGICAL AID FLUID
FDA PMA · AID, SURGICAL, VISCOELASTIC · Altacor, Ltd.
Key facts
| PMA number | P960011 |
|---|---|
| Trade name | BIOLON 1% SODIUM HYALURONATE VISCOELASTIC SURGICAL AID FLUID |
| Generic name | AID, SURGICAL, VISCOELASTIC |
| Applicant | Altacor , Ltd. |
| Owner/operator | Amring Pharmaceuticals Inc. |
| Product code | LZP |
| Approval date | Jul 16, 1998 |
| Docket number | 98M-0604 |
| Notice date | Aug 17, 1998 |
| Establishment registration | 3011965331 |
| FEI number | 3010477034 |
At a glance
- 10–99 Supplements
- Oct 3, 2022 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- No Withdrawn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: