HDE supplement
H140001 S003: IMPELLA RP SYSTEM
FDA HDE supplement · 30-day notice · ABIOMED, INC.
Key facts
| Original HDE | H140001 |
|---|---|
| Supplement number | S003 |
| Supplement type | 30-day notice |
| Reason for the supplement | process change - manufacturer/sterilizer/packager/supplier |
| Trade name | IMPELLA RP SYSTEM |
| Generic name | Right ventricular bypass (assist) device |
| Applicant | ABIOMED, INC. |
| Product code | OJE |
| Received date | Jun 5, 2015 |
| Decision date | Jul 2, 2015 |
At a glance
- No Approval order on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About HDE supplements
An HDE supplement asks FDA to approve a change to a Humanitarian Use Device that already holds a humanitarian device exemption.
Source: U.S. Food and Drug Administration (FDA), Humanitarian Device Exemption (HDE) database · Source date: