FDA 510(k) Application Details - K241410

Device Classification Name	Catheter, Conduction, Anesthetic   More FDA Info for this Device
510(K) Number	K241410
Device Name	Catheter, Conduction, Anesthetic
Applicant	JMT Co., Ltd 70-39, Gwonyul-ro 1203beon-gil, Baekseok-eup Yangju-si 11517 KR Other 510(k) Applications for this Company
Contact	Sang-Ok Nam Other 510(k) Applications for this Contact
Regulation Number	868.5120   More FDA Info for this Regulation Number
Classification Product Code	BSO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/17/2024
Decision Date	02/13/2025
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review