FDA 510(k)

NICO Myriad

K-Number: K182340 · 2018-09-20

Decision Date2018-09-20

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

NICO Myriad is a medical device manufactured by Nico Corporation. It received FDA 510(k) clearance on 2018-09-20 under approval number K182340. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NICO Myriad?

NICO Myriad is a medical device that received FDA 510(k) clearance on 2018-09-20. It is manufactured by Nico Corporation. The 510(k) number is K182340.

When was NICO Myriad approved by the FDA?

NICO Myriad received FDA 510(k) clearance on 2018-09-20, under approval number K182340.

What company makes NICO Myriad?

NICO Myriad is manufactured by Nico Corporation.

What is the FDA product code for NICO Myriad?

The FDA product code for NICO Myriad is GEI.

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K161307NICO Myriad K162075NICO TRIOwand K172433NICO BrainPath K191599NICO Myriad NOVUS K232567Myriad SPECTRA Light Source

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Official Source

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