GDY
- Product code
- GDY
- Device name
- Gauze/Sponge, Internal, X-Ray Detectable
- Device class
- Class 1
- 21 CFR
- 21 CFR 878.4450
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 111 (all years; only the last 3 years are listed here)
Official FDA classification page: GDY
Classification and pathway per current FDA publications. Data from openFDA (CC0).