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FDA 510(k)

cmTriage

K-Number: K183285 · 2019-03-08

ApplicantCuremetrix, Inc.
Decision Date2019-03-08
Product CodeQFM
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

cmTriage is a medical device manufactured by Curemetrix, Inc.. It received FDA 510(k) clearance on 2019-03-08 under approval number K183285. The device is classified under product code QFM. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the cmTriage?

cmTriage is a medical device that received FDA 510(k) clearance on 2019-03-08. It is manufactured by Curemetrix, Inc.. The 510(k) number is K183285.

When was cmTriage approved by the FDA?

cmTriage received FDA 510(k) clearance on 2019-03-08, under approval number K183285.

What company makes cmTriage?

cmTriage is manufactured by Curemetrix, Inc..

What is the FDA product code for cmTriage?

The FDA product code for cmTriage is QFM.

Other Devices by Curemetrix, Inc.

K232367cmAngio® V1.0 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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