Contour ProtégéAI+
K-Number: K250035 · 2025-02-03
ApplicantMim Software, Inc.
Decision Date2025-02-03
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 2025-02-03 under approval number K250035. 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 2025-02-03. It is manufactured by Mim Software, Inc.. The 510(k) number is K250035.
When was Contour ProtégéAI+ approved by the FDA?
Contour ProtégéAI+ received FDA 510(k) clearance on 2025-02-03, under approval number K250035.
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.
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.