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)DeviceApplicantDecision date
K834293ELECTRONIC CELL ENERGIZERElectronic Energy, Inc.1984-01-13