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FDA 510(k)

FilmArray Pneumonia Panel plus

K-Number: K181324 · 2018-11-15

Decision Date2018-11-15
Product CodeQDS
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

FilmArray Pneumonia Panel plus is a medical device manufactured by Biofire Diagnostics, LLC. It received FDA 510(k) clearance on 2018-11-15 under approval number K181324. The device is classified under product code QDS. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FilmArray Pneumonia Panel plus?

FilmArray Pneumonia Panel plus is a medical device that received FDA 510(k) clearance on 2018-11-15. It is manufactured by Biofire Diagnostics, LLC. The 510(k) number is K181324.

When was FilmArray Pneumonia Panel plus approved by the FDA?

FilmArray Pneumonia Panel plus received FDA 510(k) clearance on 2018-11-15, under approval number K181324.

What company makes FilmArray Pneumonia Panel plus?

FilmArray Pneumonia Panel plus is manufactured by Biofire Diagnostics, LLC.

What is the FDA product code for FilmArray Pneumonia Panel plus?

The FDA product code for FilmArray Pneumonia Panel plus is QDS.

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Related Devices (Code: QDS)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.