Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MindsEye Expandable Port

K-Number: K202072 · 2020-08-26

Decision Date2020-08-26
Product CodeGZT
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MindsEye Expandable Port is a medical device manufactured by Minnetronix Neuro, Inc.. It received FDA 510(k) clearance on 2020-08-26 under approval 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. It is manufactured by Minnetronix Neuro, Inc.. The 510(k) number is K202072.

When was MindsEye Expandable Port approved by the FDA?

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

What company makes MindsEye Expandable Port?

MindsEye Expandable Port is manufactured by Minnetronix Neuro, Inc..

What is the FDA product code for MindsEye Expandable Port?

The FDA product code for MindsEye Expandable Port is GZT.

Related Devices (Code: GZT)

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.