FPB
- Product code
- FPB
- Device name
- Filter, Infusion Line
- Device class
- Class 2
- 21 CFR
- 21 CFR 880.5440
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 98
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K233277 | 2024-05-10 | Hangzhou Qiantang Longyue Biotechnolog | Filter Needle for Single Use |
Official FDA classification page: FPB
Classification and pathway per current FDA publications. Data from openFDA (CC0).