510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K123905Substantially Equivalent

Cdc Human Influenza Virus Real-Time Rt-PCR Diagnostic Panel

Centers for Disease Control and Prevention, Atlanta GA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K123905 is the FDA 510(k) clearance record for CDC HUMAN INFLUENZA VIRUS REAL-TIME RT-PCR DIAGNOSTIC PANEL, a class II device, cleared for Centers for Disease Control and Prevention on under FDA product code OQW (2009 H1n1 Influenza Virus (Swine Origin), Nucleic Acid Or Antigen, Detection And Identification). FDA's definition for product code OQW reads: "2009 H1N1 influenza virus detection and identification reagents are used to directly detect and differentiate the 2009 H1N1 influenza virus in human respiratory specimens". FDA records list 30 510(k) clearances for Centers for Disease Control and Prevention, from to . As of , FDA records show no recalls naming K123905.

Clearance record

Decision date
Received
(26 days to decision)
Product code
OQW 2009 H1n1 Influenza Virus (Swine Origin), Nucleic Acid Or Antigen, Detection And Identification
Regulation
21 CFR 866.3332
Device class
Class II
Review panel
Microbiology
Applicant
Centers for Disease Control and Prevention 1600 Clifton Rd. NE (Ms C-18), Atlanta GA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OQW

Trailing 12 months

FDA records hold no clearances under product code OQW in the trailing twelve months.

FDA records show no clearances under product code OQW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code OQW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260