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 the device name listed in this FDA 510(k) record. The listed applicant is Techmah Cmf. It received FDA 510(k) clearance on 2024-07-11 under 510(k) 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. The listed applicant is Techmah Cmf. The 510(k) number is K233874.

When did tmCMF Solution receive FDA 510(k) clearance?

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

Who is the listed applicant for tmCMF Solution?

The FDA 510(k) record lists Techmah Cmf as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for tmCMF Solution?

The FDA product code for tmCMF Solution is JEY.

Other records listing Techmah Cmf as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K231520tmCMF Solution

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Official Source

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