KCY
- Product code
- KCY
- Device name
- Tourniquet, Pneumatic
- Device class
- Class 1
- 21 CFR
- 21 CFR 878.5910
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 34 (all years; only the last 3 years are listed here)
Official FDA classification page: KCY
Classification and pathway per current FDA publications. Data from openFDA (CC0).