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FDA 510(k)

cobas SARS-CoV-2 Qualitative for use on the cobas 6800/8800 Systems

K-Number: K213804 · 2022-10-22

Decision Date2022-10-22
Product CodeQQX
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

cobas SARS-CoV-2 Qualitative for use on the cobas 6800/8800 Systems is a medical device manufactured by Roche Molecular Systems, Inc.. It received FDA 510(k) clearance on 2022-10-22 under approval number K213804. The device is classified under product code QQX. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the cobas SARS-CoV-2 Qualitative for use on the cobas 6800/8800 Systems?

cobas SARS-CoV-2 Qualitative for use on the cobas 6800/8800 Systems is a medical device that received FDA 510(k) clearance on 2022-10-22. It is manufactured by Roche Molecular Systems, Inc.. The 510(k) number is K213804.

When was cobas SARS-CoV-2 Qualitative for use on the cobas 6800/8800 Systems approved by the FDA?

cobas SARS-CoV-2 Qualitative for use on the cobas 6800/8800 Systems received FDA 510(k) clearance on 2022-10-22, under approval number K213804.

What company makes cobas SARS-CoV-2 Qualitative for use on the cobas 6800/8800 Systems?

cobas SARS-CoV-2 Qualitative for use on the cobas 6800/8800 Systems is manufactured by Roche Molecular Systems, Inc..

What is the FDA product code for cobas SARS-CoV-2 Qualitative for use on the cobas 6800/8800 Systems?

The FDA product code for cobas SARS-CoV-2 Qualitative for use on the cobas 6800/8800 Systems is QQX.

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Official Source

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