LBG — Device, Fluidized Therapy, Dry Heat Class II
FDA product code LBG covers "Device, Fluidized Therapy, Dry Heat", a Class II medical device regulated under 21 CFR 890.5500. Submissions are reviewed by the Physical Medicine panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- LBG
- Device Class
- Class II
- Regulation Number
- 890.5500
- Submission Type
- Review Panel
- PM
- Medical Specialty
- Physical Medicine
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K834293 | electronic energy | ELECTRONIC CELL ENERGIZER | January 13, 1984 |