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FDA 510(k)

cmAngio® V1.0

K-Number: K232367 · 2023-10-05

ApplicantCuremetrix, Inc.
Decision Date2023-10-05
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

cmAngio® V1.0 is a medical device manufactured by Curemetrix, Inc.. It received FDA 510(k) clearance on 2023-10-05 under approval number K232367. 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® V1.0?

cmAngio® V1.0 is a medical device that received FDA 510(k) clearance on 2023-10-05. It is manufactured by Curemetrix, Inc.. The 510(k) number is K232367.

When was cmAngio® V1.0 approved by the FDA?

cmAngio® V1.0 received FDA 510(k) clearance on 2023-10-05, under approval number K232367.

What company makes cmAngio® V1.0?

cmAngio® V1.0 is manufactured by Curemetrix, Inc..

What is the FDA product code for cmAngio® V1.0?

The FDA product code for cmAngio® V1.0 is QIH.

Other Devices by Curemetrix, Inc.

K183285cmTriage K250754cmAngio® (V1.6)

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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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