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FDA 510(k)

cmAngio® (V1.6)

K-Number: K250754 · 2025-04-10

ApplicantCuremetrix, Inc.
Decision Date2025-04-10
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

cmAngio® (V1.6) is a medical device manufactured by Curemetrix, Inc.. It received FDA 510(k) clearance on 2025-04-10 under approval number K250754. 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 cmAngio® (V1.6)?

cmAngio® (V1.6) is a medical device that received FDA 510(k) clearance on 2025-04-10. It is manufactured by Curemetrix, Inc.. The 510(k) number is K250754.

When was cmAngio® (V1.6) approved by the FDA?

cmAngio® (V1.6) received FDA 510(k) clearance on 2025-04-10, under approval number K250754.

What company makes cmAngio® (V1.6)?

cmAngio® (V1.6) is manufactured by Curemetrix, Inc..

What is the FDA product code for cmAngio® (V1.6)?

The FDA product code for cmAngio® (V1.6) is QIH.

Other Devices by Curemetrix, Inc.

K183285cmTriage K232367cmAngio® V1.0

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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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