510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K861122Substantially Equivalent

The Golden Quad Test (Toxo)

Microbiological Research Corp., Bountiful UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K861122 is the FDA 510(k) clearance record for THE GOLDEN QUAD TEST (TOXO), a class II device, cleared for Microbiological Research Corp. on under FDA product code LJK (Antisera, If, Toxoplasma Gondii). FDA records list 14 510(k) clearances for Microbiological Research Corp., from to . As of , FDA records show no recalls naming K861122.

Clearance record

Decision date
Received
(314 days to decision)
Product code
LJK Antisera, If, Toxoplasma Gondii
Regulation
21 CFR 866.3780
Device class
Class II
Review panel
Microbiology
Applicant
Microbiological Research Corp. P.O. Box 308, Bountiful UT
Third party review
No

Clearances, product code LJK

Trailing 12 months

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

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