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FDA 510(k)

MindsEye Expandable Port

K-Number: K202072 · 2020-08-26

ApplicantMinnetronix Neuro, Inc.
Decision Date2020-08-26
Product CodeGZT
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MindsEye Expandable Port is the device name listed in this FDA 510(k) record. The listed applicant is Minnetronix Neuro, Inc.. It received FDA 510(k) clearance on 2020-08-26 under 510(k) number K202072. The device is classified under product code GZT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MindsEye Expandable Port?

MindsEye Expandable Port is a medical device that received FDA 510(k) clearance on 2020-08-26. The listed applicant is Minnetronix Neuro, Inc.. The 510(k) number is K202072.

When did MindsEye Expandable Port receive FDA 510(k) clearance?

MindsEye Expandable Port received FDA 510(k) clearance on 2020-08-26, under 510(k) number K202072.

Who is the listed applicant for MindsEye Expandable Port?

The FDA 510(k) record lists Minnetronix Neuro, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MindsEye Expandable Port?

The FDA product code for MindsEye Expandable Port is GZT.

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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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