POD
- Product code
- POD
- Device name
- Temporary, Internal Use Hemostatic
- Device class
- Class 2
- 21 CFR
- 21 CFR 878.4454
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K)
- Flag
- Life-sustaining / life-supporting
- 510(k) clearances (last 3 years)
- 6
FDA classification definition
Intended to control severely bleeding wounds
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K243553 | 2025-03-18 | Teleflex Medical | QuikClot Control+ Hemostatic Device |
Official FDA classification page: POD
Classification and pathway per current FDA publications. Data from openFDA (CC0).