510(k) K834293
- Device
- ELECTRONIC CELL ENERGIZER
- Applicant
- ELECTRONIC ENERGY, INC.
- 510(k) number
- K834293
- Product code
- LBG
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1984-01-13
- Date received
- 1983-12-08
- Regulation
- 890.5500
- Classification name
- Device, Fluidized Therapy, Dry Heat
- Medical specialty
- Physical Medicine
- Review panel
- Physical Medicine
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Related Records
Applicant Contact
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
Source Documents
510(k) summary PDF not indicated by FDA
Legacy Summary
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FDA Review
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