FDA 510(k) Application Details - K233019

Device Classification Name	Enzyme Immunoassay, Amphetamine   More FDA Info for this Device
510(K) Number	K233019
Device Name	Enzyme Immunoassay, Amphetamine
Applicant	Hangzhou AllTest Biotech Co.,Ltd #550, Yinhai Street Hangzhou Economic & Technological Development Area Hangzhou 310018 CN Other 510(k) Applications for this Company
Contact	Rosa Wu Other 510(k) Applications for this Contact
Regulation Number	862.3100   More FDA Info for this Regulation Number
Classification Product Code	DKZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/22/2023
Decision Date	12/13/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	TX - Clinical Toxicology
Review Advisory Committee	TX - Clinical Toxicology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review