HDE supplement
H040005 S010: KARL STORZ Fetoscopy Instruments
FDA HDE supplement · 30-day notice · KARL STORZ ENDOSCOPY-AMERICA, INC.
Key facts
| Original HDE | H040005 |
|---|---|
| Supplement number | S010 |
| Supplement type | 30-day notice |
| Reason for the supplement | process change - manufacturer/sterilizer/packager/supplier |
| Trade name | KARL STORZ Fetoscopy Instruments |
| Generic name | Amnioscope, transabdominal (fetoscope) (and accessories) |
| Applicant | KARL STORZ ENDOSCOPY-AMERICA, INC. |
| Product code | HFA |
| Received date | Oct 7, 2024 |
| Decision date | Nov 5, 2024 |
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: