Curian Campy
K-Number: K210976 · 2021-12-23
ApplicantMeridian Bioscience, Inc.
Decision Date2021-12-23
Product CodeLQP
Advisory CommitteeMI
DecisionSubstantially Equivalent
Device Summary
Curian Campy is a medical device manufactured by Meridian Bioscience, Inc.. It received FDA 510(k) clearance on 2021-12-23 under approval 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. It is manufactured by Meridian Bioscience, Inc.. The 510(k) number is K210976.
When was Curian Campy approved by the FDA?
Curian Campy received FDA 510(k) clearance on 2021-12-23, under approval number K210976.
What company makes Curian Campy?
Curian Campy is manufactured by Meridian Bioscience, Inc..
What is the FDA product code for Curian Campy?
The FDA product code for Curian Campy is LQP.
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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.