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)

Contour ProtégéAI

K-Number: K231765 · 2023-11-08

Decision Date2023-11-08
Product CodeQKB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Contour ProtégéAI is a medical device manufactured by Mim Software, Inc.. It received FDA 510(k) clearance on 2023-11-08 under approval number K231765. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Contour ProtégéAI?

Contour ProtégéAI is a medical device that received FDA 510(k) clearance on 2023-11-08. It is manufactured by Mim Software, Inc.. The 510(k) number is K231765.

When was Contour ProtégéAI approved by the FDA?

Contour ProtégéAI received FDA 510(k) clearance on 2023-11-08, under approval number K231765.

What company makes Contour ProtégéAI?

Contour ProtégéAI is manufactured by Mim Software, Inc..

What is the FDA product code for Contour ProtégéAI?

The FDA product code for Contour ProtégéAI is QKB.

Other Devices by Mim Software, Inc.

View all 19 devices →

Related Devices (Code: QKB)

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.