510(k) K220480

Device
Revogene
Applicant
Meridian Bioscience, Inc.
510(k) number
K220480
Product code
OOI
Decision
Substantially Equivalent (SESE)
Decision date
2022-07-11
Date received
2022-02-18
Regulation
862.2570
Classification name
Real Time Nucleic Acid Amplification System
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Jack Rogers
Address
3471 River Hills Dr. Cincinnati OH US 45244 45244

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code OOI#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K243922RevogeneMeridian Bioscience, Inc.2025-03-20
K222779RevogeneMeridian Bioscience, Inc.2023-01-26
K170558revogeneGenepoc, Inc.2017-05-25
K161495ARIES MI System, ARIES HSV 1&2 Assay Cassettes-Carton of 24 (IVD), ARIES HSV 1&2 Assay Protocol File Kit (IVD)Luminex Corporation2016-06-30
K160517ARIES SystemLuminex Corporation2016-04-12
K151917ARIES SystemLuminex Corporation2015-10-06
K151690Alere i Instrument, Alere i Influenza A & B, Alere i Strep AAlere Scarborough, Inc.2015-07-16
K140447BD VIPER LT SYSTEMBecton, Dickinson and Company2014-05-20
K123955QUANTSTUDIO DX REAL-TIME PCR INSTRUMENTLife Technologies Corporation2013-03-08
K113319ROTOR-GENE Q MDXQIAGEN GmbH2012-02-06
K1023143M INTEGRATED CYCLER (110V) & (220V)Focus Diagnostics, Inc.2010-10-29
K093383NUCLISENS EASYQ ENTEROVIRUS V1.1., NUCLISENS EASYQ DIRECTOR 2.6, NUCLISENS EASYQ ANALYZER, NUCLISENS MINIMAGbioMerieux, Inc.2010-07-06
K092705ABBOTT M2000SP AND ABBOTT M2000RT, MODELS 9K14-01 (G-SERIES), 9K14-02 (E-SERIES), 9K1501Abbott Molecular, Inc.2010-05-28