Sumitomo Electric Industries, 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 |
|---|
| K852959 | PO-510 TCPO2 MONITOR | November 29, 1985 |
| K811836 | PO-200 BLOOD OXYGEN MONITOR | July 27, 1981 |