Oxyheal Medical Systems, 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 |
|---|
| K163109 | OxyHeal 4000 Multiplace Hyperbaric Chamber Family | March 22, 2017 |
| K152223 | Rectangular Multiplace Hyperbaric Chamber System Product Family with Touchscreen Control System | April 29, 2016 |