Baxter Bentley Laboratories, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K905311 | DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD. | January 15, 1991 |
| K905312 | DURAFLO II HEPARIN TREATED FEMORAL CANNULAE MODELS | January 15, 1991 |
| K882892 | MEMBRANE OXYGENATOR | September 27, 1988 |