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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 the device name listed in this FDA 510(k) record. The listed applicant is Mrimath, LLC. It received FDA 510(k) clearance on 2024-08-08 under 510(k) 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. The listed applicant is Mrimath, LLC. The 510(k) number is K233822.

When did i2Contour receive FDA 510(k) clearance?

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

Who is the listed applicant for i2Contour?

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

What is the FDA product code for i2Contour?

The FDA product code for i2Contour is QIH.

Related Devices (Code: QIH)

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.

K253794Prostate CoreLucida Medical, Ltd.K252571mdprostateMediaire GmbHK253902RealGUIDE3DIEMME SRLK253835AffinityHermes Medical Solutions ABK260980cmAngio® V2.0Curemetrix, Inc.K261210Cleerly PlaqueCleerly, Inc.

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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