FDA 510(k)

Curian Campy

K-Number: K210976 · 2021-12-23

Decision Date2021-12-23

Product CodeLQP

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

Curian Campy is the device name listed in this FDA 510(k) record. The listed applicant is Meridian Bioscience, Inc.. It received FDA 510(k) clearance on 2021-12-23 under 510(k) number K210976. The device is classified under product code LQP. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Curian Campy?

Curian Campy is a medical device that received FDA 510(k) clearance on 2021-12-23. The listed applicant is Meridian Bioscience, Inc.. The 510(k) number is K210976.

When did Curian Campy receive FDA 510(k) clearance?

Curian Campy received FDA 510(k) clearance on 2021-12-23, under 510(k) number K210976.

Who is the listed applicant for Curian Campy?

The FDA 510(k) record lists Meridian Bioscience, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Curian Campy?

The FDA product code for Curian Campy is LQP.

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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.