FHO
- Product code
- FHO
- Device name
- Pneumoperitoneum Needle
- Device class
- Class 2
- 21 CFR
- 21 CFR 876.1500
- Medical specialty
- Gastroenterology, Urology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (all years, FDA)
- 15 (all years; only the last 3 years are listed here)
FDA classification definition
For establishment of a pneumoperitoneum in abdomen.
Official FDA classification page: FHO
Classification and pathway per current FDA publications. Data from openFDA (CC0).