KDQ
- Product code
- KDQ
- Device name
- Bottle, Collection, Vacuum
- Device class
- Class 2
- 21 CFR
- 21 CFR 880.6740
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 48 (all years; only the last 3 years are listed here)
Official FDA classification page: KDQ
Classification and pathway per current FDA publications. Data from openFDA (CC0).