510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K792559Substantially Equivalent

Fiax Test Kit for Herpes Simplex Virus

Intl. Diagnostic Technology, Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K792559 is the FDA 510(k) clearance record for FIAX TEST KIT FOR HERPES SIMPLEX VIRUS, a class II device, cleared for Intl. Diagnostic Technology on under FDA product code GQL (Antisera, Fluorescent, Herpesvirus Hominis 1,2). FDA records list 29 510(k) clearances for Intl. Diagnostic Technology, from to . As of , FDA records show no recalls naming K792559.

Clearance record

Decision date
Received
(83 days to decision)
Product code
GQL Antisera, Fluorescent, Herpesvirus Hominis 1,2
Regulation
21 CFR 866.3305
Device class
Class II
Review panel
Microbiology
Applicant
Intl. Diagnostic Technology 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code GQL

Trailing 12 months

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

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