cobas® Cdiff Nucleic acid test for use on the cobas® Liat® System (07454945190); cobas® Cdiff Positive and Negative Control Kit for use on the cobas® Liat® System (07454970190)

FDA 510(k) K260045 · Roche Molecular Systems, Inc.

Substantially Equivalent

510(k) numberK260045

Submission

Device name
cobas® Cdiff Nucleic acid test for use on the cobas® Liat® System (07454945190); cobas® Cdiff Positive and Negative Control Kit for use on the cobas® Liat® System (07454970190)
Applicant
Roche Molecular Systems, Inc.
Pleasanton, CA, US
Received
January 7, 2026
Decision date
August 28, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OZN – C. Difficile Toxin Gene Amplification Assay
Device class
Class II (moderate risk)
Regulation
21 CFR 866.3130
Specialty
Microbiology

Amplification assay for the detection of c. Difficile toxin genes from stool specimens of symptomatic patients.

Other 510(k)s with product code OZN

510(k)DeviceApplicantDecision
K243730Xpert C. difficile/EpiOZN · Traditional Cepheid®02/28/2025SE
K232092Great Basin Toxigenic C. difficile Direct Test (CDF2)OZN · Traditional Vela Operations USA11/14/2023SE
K212427cobas Cdiff nucleic acid test for use on the cobas Liat SystemOZN · Special Roche Molecular Systems, Inc.10/20/2021SE
K210385cobas Cdiff nucleic acid test for use on the cobas Liat SystemOZN · Special Roche Molecular Systems, Inc.09/09/2021SE
K172569GenePOC CDiffOZN · Traditional Genepoc, Inc.11/22/2017SE
K171770cobas Cdiff Nucleic acid test for use on the cobas Liat SystemOZN · Traditional Roche Molecular Systems, Inc.09/12/2017SE
K171441ARIES C. difficile Assay Complete Kit, ARIES C. difficile Assay Protocol File Kit, ARIES…OZN · Traditional Luminex Corporation07/21/2017SE
K170491Solana C. difficile AssayOZN · Traditional Quidel Corporation05/11/2017SE
K163085Simplexa C. difficile Direct; Simplexa C. difficile Positive Control PackOZN · Traditional Focus Diagnostics, Inc.:Dba Diasorin Molecular…02/14/2017SE
K142422cobas Cdiff TestOZN · Traditional Roche Molecular Systems, Inc.05/20/2015SE

More from Roche Molecular Systems, Inc.

510(k)DeviceDecision
K260047cobas Strep A Nucleic acid test for use on the cobas Liat System (07341911190); cobas…PGX · Traditional 08/28/2026SE
K260021cobas® BV/CVPQA · Traditional 07/16/2026SE
K260917cobas CT/NG for use on the cobas 5800/6800/8800 systems; cobas TV/MG for use on the…QEP · Traditional 07/08/2026SE
K253759cobas liat CT/NG/MG nucleic acid testQEP · Dual Track 05/15/2026SE
K253756cobas liat CT/NG nucleic acid testQEP · Dual Track 05/15/2026SE
K243753cobas liat Bordetella panel nucleic acid testOZZ · Dual Track 11/20/2025SE
K252484cobas HCVMZP · Traditional 11/03/2025SE
K252481cobas CMVPAB · Traditional 11/03/2025SE
K243455cobas Respiratory 4-flex for use on the cobas 5800/6800/8800 SystemsQOF · Traditional 07/31/2025SE
K243863Opulus™ Lymphoma PrecisionQIH · Traditional 05/30/2025SE

Questions and answers

When was cobas® Cdiff Nucleic acid test for use on the cobas® Liat® System (07454945190); cobas® Cdiff Positive and Negative Control Kit for use on the cobas® Liat® System (07454970190) cleared by the FDA?

cobas® Cdiff Nucleic acid test for use on the cobas® Liat® System (07454945190); cobas® Cdiff Positive and Negative Control Kit for use on the cobas® Liat® System (07454970190) (K260045) received a 510(k) decision of Substantially Equivalent on August 28, 2026, 233 days after the submission was received.

What is the product code of K260045?

The FDA product code is OZN – C. Difficile Toxin Gene Amplification Assay, a Class II (moderate risk) device regulated under 21 CFR 866.3130.