FDA 510(k) Application Details - K150266

Device Classification Name	Needle, Conduction, Anesthetic (W/Wo Introducer)   More FDA Info for this Device
510(K) Number	K150266
Device Name	Needle, Conduction, Anesthetic (W/Wo Introducer)
Applicant	REMINGTON MEDICAL, INC. 6830 MEADOWRIDGE COURT ALPHARETTA, GA 30005 US Other 510(k) Applications for this Company
Contact	CAITLIN SENTER 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	02/04/2015
Decision Date	06/04/2015
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