CAD
- Product code
- CAD
- Device name
- Vaporizer, Anesthesia, Non-Heated
- Device class
- Class 2
- 21 CFR
- 21 CFR 868.5880
- Medical specialty
- Anesthesiology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 57
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K240375 | 2024-10-31 | Shenzhen Mindray Bio-Medical Electroni | V80 Anesthetic Vaporizer (V80) |
Official FDA classification page: CAD
Classification and pathway per current FDA publications. Data from openFDA (CC0).