510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K222829Substantially Equivalent

Curian® Shiga Toxin

Meridian Bioscience Inc, Cincinnati OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K222829 is the FDA 510(k) clearance record for Curian® Shiga Toxin, a class I device, cleared for Meridian Bioscience, Inc. on under FDA product code GMZ (Antigens, All Types, Escherichia Coli). FDA records list 38 510(k) clearances for Meridian Bioscience, Inc., from to . As of , FDA records show no recalls naming K222829.

Clearance record

Decision date
Received
(210 days to decision)
Product code
GMZ Antigens, All Types, Escherichia Coli
Regulation
21 CFR 866.3255
Device class
Class I
Review panel
Microbiology
Applicant
Meridian Bioscience, Inc. 3471 River Hills Dr., Cincinnati OH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GMZ

Trailing 12 months

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

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