FDA 510(k)

NICO Myriad

K-Number: K161307 · 2016-12-21

Decision Date2016-12-21

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 2016-12-21 under approval number K161307. 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 2016-12-21. It is manufactured by Nico Corporation. The 510(k) number is K161307.

When was NICO Myriad approved by the FDA?

NICO Myriad received FDA 510(k) clearance on 2016-12-21, under approval number K161307.

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.

Other Devices by Nico Corporation

K162075NICO TRIOwand K172433NICO BrainPath K182340NICO Myriad K191599NICO Myriad NOVUS K232567Myriad SPECTRA Light Source

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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.