PMA supplement
P840040 S002: MEDI-TECH CORONARY BALLOON DILATATION CATHETER SYS
FDA PMA supplement · Boston Scientific Corp
Key facts
| Original PMA | P840040 |
|---|---|
| Supplement number | S002 |
| Trade name | MEDI-TECH CORONARY BALLOON DILATATION CATHETER SYS |
| Generic name | Catheters, transluminal coronary angioplasty, percutaneous |
| Applicant | Boston Scientific Corp |
| Product code | LOX |
| Received date | Feb 21, 1986 |
| Decision date | Jul 11, 1986 |
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: