FDA 510(k) Application Details - K202492

Device Classification Name	Needle, Hypodermic, Single Lumen   More FDA Info for this Device
510(K) Number	K202492
Device Name	Needle, Hypodermic, Single Lumen
Applicant	Teleflex Medical 3015 Carrington Mill Blvd. Morrisville, NC 27560 US Other 510(k) Applications for this Company
Contact	Rachel Rehl Other 510(k) Applications for this Contact
Regulation Number	880.5570   More FDA Info for this Regulation Number
Classification Product Code	FMI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/31/2020
Decision Date	03/22/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review