cobas SARS-CoV-2 Qualitative for use on the cobas 6800/8800 Systems
K-Number: K213804 · 2022-10-22
Device Summary
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.
Related Clinical Trials
Other Devices by Roche Molecular Systems, Inc.
Related Devices (Code: QQX)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.