PMA
P050038: ARISTA AH ABSORBABLE HEMOSTAT
FDA PMA · Agent, absorbable hemostatic, non-collagen based · Davol, Inc.
Key facts
| PMA number | P050038 |
|---|---|
| Trade name | ARISTA AH ABSORBABLE HEMOSTAT |
| Generic name | Agent, absorbable hemostatic, non-collagen based |
| Applicant | Davol, Inc. |
| Owner/operator | C. R. Bard, Inc. |
| Product code | LMG |
| Approval date | Sep 26, 2006 |
| Docket number | 06M-0396 |
| Notice date | Oct 3, 2006 |
| Establishment registration | 1213643 |
| FEI number | 1213643 |
At a glance
- 10–99 Supplements
- Jul 15, 2026 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- 10–99 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: