FQO
- Product code
- FQO
- Device name
- Table, Operating-Room, Ac-Powered
- Device class
- Class 1
- 21 CFR
- 21 CFR 878.4960
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 35
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name |
|---|---|---|---|
| K240598 | 2024-06-03 | Moon Surgical | Maestro System (REF100) summary |
Official FDA classification page: FQO
Classification and pathway per current FDA publications. Data from openFDA (CC0).