510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K220480Substantially Equivalent

Revogene

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

K220480 is the FDA 510(k) clearance record for Revogene, a class II device, cleared for Meridian Bioscience, Inc. on under FDA product code OOI (Real Time Nucleic Acid Amplification System). FDA's definition for product code OOI reads: "The system is a clinical multiplex instrument intended to measure and sort multiple signals generated my multiple probes, intercalating dyes, or other ligands in an assay from a clinical sample. Signals may be generated by fluorescence or...". FDA records list 38 510(k) clearances for Meridian Bioscience, Inc., from to . As of , FDA records show no recalls naming K220480.

Clearance record

Decision date
Received
(143 days to decision)
Product code
OOI Real Time Nucleic Acid Amplification System
Regulation
21 CFR 862.2570
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Meridian Bioscience, Inc. 3471 River Hills Dr., Cincinnati OH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OOI

Trailing 12 months

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

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