Douglas Scientific Products
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K813174 | BRADYCARDIA ALARM | January 22, 1982 |
| K802710 | INFANT APNEA MONITOR | November 12, 1980 |