PMA supplement
P780011 S012: MINI BALLOON
FDA PMA supplement · Normal 180 Day Track · Bd Becton Dickinson Vacutainer Systems Preanalytic
Key facts
| Original PMA | P780011 |
|---|---|
| Supplement number | S012 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | MINI BALLOON |
| Generic name | Device, Vascular, for Promoting Embolization |
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic |
| Product code | KRD |
| Received date | Aug 29, 1989 |
| Decision date | Oct 30, 1989 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: