KDP
- Product code
- KDP
- Device name
- Regulator, Vacuum
- Device class
- Class 2
- 21 CFR
- 21 CFR 880.6740
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 21
Official FDA classification page: KDP
Classification and pathway per current FDA publications. Data from openFDA (CC0).