FDA 510(k), K152967, NERBRIDGE

510(K) Number: K152967
Device Name: NERBRIDGE
Manufacturer: TOYOBO CO., LTD.
Device Classification Name: Cuff, Nerve
Regulation Number: 882.5275
Classification Product Code: JXI
Date Received: 10/08/2015
Decision Date: 06/22/2016
Regulation Medical Specialty: Neurology

494 pages (1,748 of 2,242 original pages are fully redacted)