LBG
- Product code
- LBG
- Device name
- Device, Fluidized Therapy, Dry Heat
- Device class
- Class 2
- 21 CFR
- 21 CFR 890.5500
- Medical specialty
- Physical Medicine
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (all years, FDA)
- 1 (all years; only the last 3 years are listed here)
Official FDA classification page: LBG
Classification and pathway per current FDA publications. Data from openFDA (CC0).