FDA 510(k) Application Details - K243274

Device Classification Name	More FDA Info for this Device
510(K) Number	K243274
Device Name	CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel: Influenza A/B Typing Kit (VER 2); Influenza A SubTyping Kit (VER 4); Influenza B Genotyping Kit (VER 1.1 and 2); and Influenza A/H5 Subtyping Kit (VER 4)
Applicant	Centers for Disease Control and Prevention 1600 Clifton Road Atlanta, GA 30329 US Other 510(k) Applications for this Company
Contact	Marie Kirby Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OZE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/16/2024
Decision Date	07/11/2025
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review