MDB
- Product code
- MDB
- Device name
- System, Blood Culturing
- Device class
- Class 1
- 21 CFR
- 21 CFR 866.2560
- Medical specialty
- Microbiology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 1
- Summaries archived here
- 1 (direct download)
- 510(k) clearances (all years, FDA)
- 68 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K260213 | 2026-05-28 | BD Diagnostic Systems | BD BACTEC FXI Culture System |
Official FDA classification page: MDB
Classification and pathway per current FDA publications. Data from openFDA (CC0).