FEG
- Product code
- FEG
- Device name
- Tube, Double Lumen For Intestinal Decompression And/Or Intubation
- Device class
- Class 2
- 21 CFR
- 21 CFR 876.5980
- Medical specialty
- Gastroenterology, Urology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 13
Official FDA classification page: FEG
Classification and pathway per current FDA publications. Data from openFDA (CC0).