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FDA 510(k)

EIDON FA

K-Number: K180526 · 2018-07-16

ApplicantCentervue S.P.A.
Decision Date2018-07-16
Product CodeMYC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

EIDON FA is a medical device manufactured by Centervue S.P.A.. It received FDA 510(k) clearance on 2018-07-16 under approval number K180526. The device is classified under product code MYC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EIDON FA?

EIDON FA is a medical device that received FDA 510(k) clearance on 2018-07-16. It is manufactured by Centervue S.P.A.. The 510(k) number is K180526.

When was EIDON FA approved by the FDA?

EIDON FA received FDA 510(k) clearance on 2018-07-16, under approval number K180526.

What company makes EIDON FA?

EIDON FA is manufactured by Centervue S.P.A..

What is the FDA product code for EIDON FA?

The FDA product code for EIDON FA is MYC.

Other Devices by Centervue S.P.A.

K153181MAIA K180293Retia 2 K192113DRSplus K213705DRSplus K211328EIDON FA, EIDON, EIDON AF, EIDON UWFL K234076iCare ALTIUS CW

View all 8 devices →

Related Devices (Code: MYC)

K153181MAIACentervue S.P.A. K180293Retia 2Centervue S.P.A. K192113DRSplusCentervue S.P.A. K213705DRSplusCentervue S.P.A. K211328EIDON FA, EIDON, EIDON AF, EIDON UWFLCentervue S.P.A. K241931OcuMet Beacon (OCUB100)Ocusciences, Inc.

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.

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