FDA 510(k) Application Details - K170112

Device Classification Name	Needle, Conduction, Anesthetic (W/Wo Introducer)   More FDA Info for this Device
510(K) Number	K170112
Device Name	Needle, Conduction, Anesthetic (W/Wo Introducer)
Applicant	INTERNATIONAL MEDICAL DEVELOPMENT, INC.(IMD) 560 HIGHWAY 39 (PO BOX 510) HUNTSVILLE, UT 84317 US Other 510(k) Applications for this Company
Contact	WALTER ZOHMANN Other 510(k) Applications for this Contact
Regulation Number	868.5150   More FDA Info for this Regulation Number
Classification Product Code	BSP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/12/2017
Decision Date	02/02/2018
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