510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K852931Substantially Equivalent

Herpes Hominus I-Comple Fix Antigen & Negative Clt

Microbix Biosystems, Inc., Canada, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K852931 is the FDA 510(k) clearance record for HERPES HOMINUS I-COMPLE FIX ANTIGEN & NEGATIVE CLT, a class II device, cleared for Microbix Biosystems, Inc. on under FDA product code GQO (Antisera, Cf, Herpesvirus Hominis 1,2). FDA records list 7 510(k) clearances for Microbix Biosystems, Inc., from to . As of , FDA records show no recalls naming K852931.

Clearance record

Decision date
Received
(126 days to decision)
Product code
GQO Antisera, Cf, Herpesvirus Hominis 1,2
Regulation
21 CFR 866.3305
Device class
Class II
Review panel
Microbiology
Applicant
Microbix Biosystems, Inc. 341 Bering Ave., Canada, CA
Third party review
No

Clearances, product code GQO

Trailing 12 months

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

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