510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K903882Substantially Equivalent

Varicella-Zoster Virus Antibody Test Kit-Latex Agg

Viral Antigens, Inc., Memphis TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K903882 is the FDA 510(k) clearance record for VARICELLA-ZOSTER VIRUS ANTIBODY TEST KIT-LATEX AGG, a class II device, cleared for Viral Antigens, Inc. on under FDA product code GQW (Antigen, Cf, (Including Cf Control), Varicella-Zoster). FDA records list 6 510(k) clearances for Viral Antigens, Inc., from to . As of , FDA records show no recalls naming K903882.

Clearance record

Decision date
Received
(104 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
Viral Antigens, Inc. 5171 Wilfong Rd., Memphis TN
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