KCQ
- Product code
- KCQ
- Device name
- Tube Impression And Matrix
- Device class
- Class 1
- 21 CFR
- 21 CFR 872.6570
- Medical specialty
- Dental
- Marketing pathway
- 510(K) Exempt
- Flag
- GMP exempt
- 510(k) clearances (last 3 years)
- 1
Official FDA classification page: KCQ
Classification and pathway per current FDA publications. Data from openFDA (CC0).