FDA 510(k) Application Details - K233322

Device Classification Name	Cuff, Nerve   More FDA Info for this Device
510(K) Number	K233322
Device Name	Cuff, Nerve
Applicant	Mochida Pharmaceutical Co., Ltd. 1-7 Yotsuya Shinjuku-ku 160-8515 JP Other 510(k) Applications for this Company
Contact	Akiko Koarai Other 510(k) Applications for this Contact
Regulation Number	882.5275   More FDA Info for this Regulation Number
Classification Product Code	JXI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/29/2023
Decision Date	06/21/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review