FDA 510(k), K201290, Medline DeNovo 4Pro Electrical Stimulation Device

510(K) Number: K201290
Device Name: Medline DeNovo 4Pro Electrical Stimulation Device
Manufacturer: Medline Industries Inc
Device Classification Name: Stimulator, Muscle, Powered
Regulation Number: 890.5850
Classification Product Code: IPF
Date Received: 05/14/2020
Decision Date: 09/21/2020
Regulation Medical Specialty: Physical Medicine

613 pages (2,305 of 2,918 original pages are fully redacted)