Product code LBG— Physical Medicine

ELECTRONIC CELL ENERGIZER

Classification name: Device, Fluidized Therapy, Dry Heat
Device class: Class 2
Regulation: 21 CFR 890.5500
Advisory panel: Physical Medicine
Total cleared: 1
First cleared: 1984-01-13
Most recent: 1984-01-13

Market context for product code LBG

FDA has cleared 1 device under product code LBG, all in 1984, filed by 1 applicant company. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Top applicants under product code LBG

Electronic Energy, Inc.1 clearance

Recent clearances under product code LBG

K834293 — ELECTRONIC CELL ENERGIZERElectronic Energy, Inc.·1984-01-13

Data sourced from openFDA. This site is unofficial and independent of the FDA.