FDA 510(k)

tmCMF Solution

K-Number: K233874 · 2024-07-11

Decision Date2024-07-11

Product CodeJEY

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

tmCMF Solution is a medical device manufactured by Techmah Cmf. It received FDA 510(k) clearance on 2024-07-11 under approval number K233874. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the tmCMF Solution?

tmCMF Solution is a medical device that received FDA 510(k) clearance on 2024-07-11. It is manufactured by Techmah Cmf. The 510(k) number is K233874.

When was tmCMF Solution approved by the FDA?

tmCMF Solution received FDA 510(k) clearance on 2024-07-11, under approval number K233874.

What company makes tmCMF Solution?

tmCMF Solution is manufactured by Techmah Cmf.

What is the FDA product code for tmCMF Solution?

The FDA product code for tmCMF Solution is JEY.

Other Devices by Techmah Cmf

K231520tmCMF Solution

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.