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FDA 510(k)

i2Contour

K-Number: K233822 · 2024-08-08

ApplicantMrimath, LLC
Decision Date2024-08-08
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

i2Contour is a medical device manufactured by Mrimath, LLC. It received FDA 510(k) clearance on 2024-08-08 under approval number K233822. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the i2Contour?

i2Contour is a medical device that received FDA 510(k) clearance on 2024-08-08. It is manufactured by Mrimath, LLC. The 510(k) number is K233822.

When was i2Contour approved by the FDA?

i2Contour received FDA 510(k) clearance on 2024-08-08, under approval number K233822.

What company makes i2Contour?

i2Contour is manufactured by Mrimath, LLC.

What is the FDA product code for i2Contour?

The FDA product code for i2Contour is QIH.

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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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