510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K183462Substantially Equivalent

Applied Biosystems Bacillus anthracis Detection Kit

Mriglobal, Kansas City MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K183462 is the FDA 510(k) clearance record for Applied Biosystems Bacillus anthracis Detection Kit, cleared for Mriglobal on under FDA product code QIF. FDA records list one 510(k) clearance for Mriglobal. As of , FDA records show no recalls naming K183462.

Clearance record

Decision date
Received
(291 days to decision)
Product code
QIF
Review panel
Immunology
Applicant
Mriglobal 425 Volker Blvd., Kansas City MO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QIF

Trailing 12 months

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

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