PMA
P010049: QUICKSEAL FEMORAL ARTERIAL CLOSURE SYSTEM
FDA PMA · Device, hemostasis, vascular · Sub-Q, Inc.
Key facts
| PMA number | P010049 |
|---|---|
| Trade name | QUICKSEAL FEMORAL ARTERIAL CLOSURE SYSTEM |
| Generic name | Device, hemostasis, vascular |
| Applicant | Sub-Q, Inc. |
| Product code | MGB |
| Approval date | Mar 25, 2002 |
| Docket number | 02M-0134 |
| Notice date | Mar 29, 2002 |
| FEI number | 3004145492 |
At a glance
- 10–99 Supplements
- Aug 31, 2004 Latest supplement decision
- No Withdrawn
- Yes 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: