KDT
- Product code
- KDT
- Device name
- Container, Specimen Mailer And Storage, Sterile
- Device class
- Class 1
- 21 CFR
- 21 CFR 864.3250
- Medical specialty
- Pathology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 12
Official FDA classification page: KDT
Classification and pathway per current FDA publications. Data from openFDA (CC0).