B. Braun Instruments
B. Braun Instruments appears in FDA public data with 0 recalls, 13 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 2, 1976.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 13
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K760390 | CATHETER, VEIN (BRAUNULA T) | November 2, 1976 |
| K760388 | CATHETER, VEIN (VENOFIX) | November 2, 1976 |
| K760384 | STOPPERS | November 2, 1976 |
| K760389 | CANNULA, IV | November 2, 1976 |
| K760381 | BLOOD TRANSFUSION SET (SANGOFIX) | November 2, 1976 |
| K760382 | CONNECTORS | November 2, 1976 |
| K760385 | EXTENSION SETS | November 2, 1976 |
| K760386 | CENTRAL VEINOUS PRESSURE SETS | November 2, 1976 |
| K760387 | CATHETER, CAVA (CAVAFIX) | November 2, 1976 |
| K760391 | CATHETER, VEIN (BRAUNULA) | November 2, 1976 |
| K760383 | STOPCOCKS | November 2, 1976 |
| K760380 | INTRAVENOUS TRANSFER SET (INTRAFIX) | November 2, 1976 |
| K760392 | SYRINGES | November 2, 1976 |