510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K942743Substantially Equivalent

Viro Varicella-Zoster Virus Identification Reagent

Viro Research LLC, Rockford IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K942743 is the FDA 510(k) clearance record for VIRO VARICELLA-ZOSTER VIRUS IDENTIFICATION REAGENT, a class II device, cleared for Viro Research, Inc. on under FDA product code GQW (Antigen, Cf, (Including Cf Control), Varicella-Zoster). FDA records list one 510(k) clearance for Viro Research, Inc. As of , FDA records show no recalls naming K942743.

Clearance record

Decision date
Received
(188 days to decision)
Product code
GQW Antigen, Cf, (Including Cf Control), Varicella-Zoster
Regulation
21 CFR 866.3900
Device class
Class II
Review panel
Microbiology
Applicant
Viro Research, Inc. 5301 E. State St., #307a, Rockford IL
510(k) summary
Summary
Third party review
No

Clearances, product code GQW

Trailing 12 months

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

FDA records show no clearances under product code GQW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GQW, 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