LFF
- Product code
- LFF
- Device name
- Unit, Activation, Breath Control
- Device class
- Class 1
- 21 CFR
- 21 CFR 890.3920
- Medical specialty
- Physical Medicine
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 1
Official FDA classification page: LFF
Classification and pathway per current FDA publications. Data from openFDA (CC0).