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FDA 510(k)

NICO Myriad

K-Number: K161307 · 2016-12-21

ApplicantNico Corporation
Decision Date2016-12-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NICO Myriad is the device name listed in this FDA 510(k) record. The listed applicant is Nico Corporation. It received FDA 510(k) clearance on 2016-12-21 under 510(k) 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. The listed applicant is Nico Corporation. The 510(k) number is K161307.

When did NICO Myriad receive FDA 510(k) clearance?

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

Who is the listed applicant for NICO Myriad?

The FDA 510(k) record lists Nico Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NICO Myriad?

The FDA product code for NICO Myriad is GEI.

Other records listing Nico Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K232567Myriad SPECTRA Light SourceK191599NICO Myriad NOVUSK182340NICO MyriadK172433NICO BrainPathK162075NICO TRIOwand

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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.

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