FDA 510(k) Application Details - K231724

Device Classification Name	Saline, Vascular Access Flush   More FDA Info for this Device
510(K) Number	K231724
Device Name	Saline, Vascular Access Flush
Applicant	SPM Medicare Pvt. Ltd. B-40, Phase II Noida, Gautam Budh Nagar 201305 IN Other 510(k) Applications for this Company
Contact	Sanjay Kumar Other 510(k) Applications for this Contact
Regulation Number	880.5200   More FDA Info for this Regulation Number
Classification Product Code	NGT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/13/2023
Decision Date	11/09/2023
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