Medrad, Inc. / Bayer Medical Care, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K132928 | MEDRAD MARK 7 ARTERION INJECTION SYSTEM / SYRINGE, TWIST & GO SYRINGE | January 23, 2014 |
| K131517 | MEDRAD TWIST & GO HIGH PRESSURE CONNECTOR TUBING | August 2, 2013 |