FDA Review Panel · MI

FDA 510(k) Microbiology Devices

About Microbiology Devices

FDA 510(k) microbiology devices include diagnostic systems used to detect and identify bacteria, viruses, fungi and parasites. The FDA review panel code is MI.

Key device types:

  • Blood culture systems - automated incubation and detection platforms
  • Microbial identification - MALDI-TOF, biochemical and molecular ID systems
  • Antimicrobial susceptibility testing - MIC determination and breakpoint analysis
  • Rapid infectious disease tests - influenza, strep, RSV, COVID-19 antigen and molecular tests
  • Molecular diagnostics - PCR panels for respiratory, GI and STI pathogens

7038
Total
6976
Cleared
102d
Avg days
1976
Since

FDA 510(k) Cleared Microbiology Devices

This page lists all 7038 medical devices in the Microbiology specialty that have been submitted to the FDA through the 510(k) premarket notification process. Culture systems, microbial identification and infectious disease test kits.

  • 6976 devices cleared as substantially equivalent to a predicate device.
  • Average time to FDA decision: 102 days.
  • Records available from 1976 to the present.
  • Filter by product code using the sidebar to narrow results by device type.
363 Microbiology devices
1–12 of 363
Cleared May 01, 2026
BioCode® Respiratory Pathogen Panel (RPP)
K254139 · Applied BioCode, Inc.
OCC · Respiratory Virus Panel Nucleic Acid Assay System · 130d
Cleared Apr 30, 2026
AllTest Strep A Rapid Test
K260342 · Hangzhou AllTest Biotech Co., Ltd.
GTY · Antigens, All Groups, Streptococcus Spp. · 87d
Cleared Apr 28, 2026
Anti-HCV Next
K252424 · Abbott Laboratories
MZO · Assay, Enzyme Linked Immunosorbent, Hepatitis C Virus · 270d
Cleared Apr 21, 2026
ETEST Gepotidacin (GEP) (0.016-256 µg/mL)
K260447 · Biom?rieux SA
JWY · Manual Antimicrobial Susceptibility Test Systems · 69d
Cleared Apr 17, 2026
MTS Gepotidacin 0.016-256 µg/mL
K260696 · Liofilchem S. R. L.
JWY · Manual Antimicrobial Susceptibility Test Systems · 45d
Cleared Apr 15, 2026
VITEK 2 AST-Streptococcus Inducible Clindamycin Resistance
K260282 · bioMerieux, Inc.
LON · System, Test, Automated, Antimicrobial Susceptibility, Short Incubation · 76d
Cleared Apr 15, 2026
ASTar BC G- Kit
K253573 · Q-Linea AB
SAN · Automated Antimicrobial Susceptibility Test System For Positive Blood Culture Samples · 149d
Cleared Apr 13, 2026
Heal-Check Rapid COVID-19 Antigen Self-Test
K260095 · Healgen Scientific, LLC
QYT · Over-the-counter Covid-19 Antigen Test · 90d
Cleared Apr 13, 2026
Elecsys Anti-SARS-CoV-2 S
K252280 · Roche Diagnostics
QVP · Sars-cov-2 Serology Test · 265d
Cleared Apr 07, 2026
Elecsys Anti-HBc IgM
K260049 · Roche Diagnostics
SEI · Qualitative And Quantitative Hepatitis B Virus Antibody Assays · 90d
Cleared Apr 07, 2026
Elecsys Anti-HAV IgM
K260048 · Roche Diagnostics
LOL · Hepatitis A Test (antibody And Igm Antibody) · 90d
Cleared Apr 07, 2026
Elecsys Anti-HBc II
K260046 · Roche Diagnostics
SEI · Qualitative And Quantitative Hepatitis B Virus Antibody Assays · 90d

How to use this database

This page lists 7038 medical devices in the Microbiology specialty submitted to the FDA through the 510(k) premarket notification process. Of these, 6976 were cleared as substantially equivalent to a predicate device. Average FDA review time: 102 days. Records from 1976 to the present.

You can use this list to:

  • Find predicate devices for a new 510(k) submission
  • Verify the clearance status of a specific device
  • Identify FDA product codes related to microbiology
  • Compare similar cleared devices within this category
  • Research manufacturers active in this specialty

Each entry includes: device name, 510(k) number, product code, manufacturer and FDA decision date. Click any device to view the full submission details.

This information is based on publicly available FDA data and is intended for informational purposes only. It may not reflect current market or regulatory status. Always verify critical information at accessdata.fda.gov.

Looking for a specific microbiology device? Search by device name, K-number or manufacturer.

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