HDE supplement
H080005 S001: ELANA ARTERIOTOMY SYSTEM
FDA HDE supplement · normal 75 day track · ELANA INC.
Key facts
| Original HDE | H080005 |
|---|---|
| Supplement number | S001 |
| Supplement type | normal 75 day track |
| Reason for the supplement | location change - manufacturer/sterilizer/packager/supplier |
| Trade name | ELANA ARTERIOTOMY SYSTEM |
| Generic name | Catheter, peripheral, atherectomy |
| Applicant | ELANA INC. |
| Product code | MCW |
| Received date | Jun 15, 2011 |
| Decision date | Sep 15, 2011 |
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: