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FDA 510(k)

NICO TRIOwand

K-Number: K162075 · 2016-08-11

ApplicantNico Corporation
Decision Date2016-08-11
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NICO TRIOwand is a medical device manufactured by Nico Corporation. It received FDA 510(k) clearance on 2016-08-11 under approval number K162075. 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 TRIOwand?

NICO TRIOwand is a medical device that received FDA 510(k) clearance on 2016-08-11. It is manufactured by Nico Corporation. The 510(k) number is K162075.

When was NICO TRIOwand approved by the FDA?

NICO TRIOwand received FDA 510(k) clearance on 2016-08-11, under approval number K162075.

What company makes NICO TRIOwand?

NICO TRIOwand is manufactured by Nico Corporation.

What is the FDA product code for NICO TRIOwand?

The FDA product code for NICO TRIOwand is GEI.

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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.

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