Intuit Medical Products, LLC
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K181546 | Dillard Nasal Balloon Catheter | January 3, 2020 |
| K153484 | Dillard Airway Dilatation System | July 27, 2016 |
| K143738 | DSS Sinusplasty Balloon Catheter | August 27, 2015 |