Product code LBG
- Device name
- Device, Fluidized Therapy, Dry Heat
- Medical specialty
- Physical Medicine
- Device class
- 2
- Regulation number
- 890.5500
- Review panel
- PM
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- Y
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset
Related 510(k) Records
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K834293 | ELECTRONIC CELL ENERGIZER | Electronic Energy, Inc. | 1984-01-13 |