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FDA 510(k)

cobas liat CT/NG nucleic acid test

K-Number: K253756 · 2026-05-15

Decision Date2026-05-15
Product CodeQEP
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

cobas liat CT/NG nucleic acid test is a medical device manufactured by Roche Molecular Systems, Inc.. It received FDA 510(k) clearance on 2026-05-15 under approval number K253756. The device is classified under product code QEP. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the cobas liat CT/NG nucleic acid test?

cobas liat CT/NG nucleic acid test is a medical device that received FDA 510(k) clearance on 2026-05-15. It is manufactured by Roche Molecular Systems, Inc.. The 510(k) number is K253756.

When was cobas liat CT/NG nucleic acid test approved by the FDA?

cobas liat CT/NG nucleic acid test received FDA 510(k) clearance on 2026-05-15, under approval number K253756.

What company makes cobas liat CT/NG nucleic acid test?

cobas liat CT/NG nucleic acid test is manufactured by Roche Molecular Systems, Inc..

What is the FDA product code for cobas liat CT/NG nucleic acid test?

The FDA product code for cobas liat CT/NG nucleic acid test is QEP.

Other Devices by Roche Molecular Systems, Inc.

Related Devices (Code: QEP)

Official Source

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