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FDA 510(k)

U-MAT

K-Number: K790466 · 1979-03-28

ApplicantEngineering Dynamics Corp.
Decision Date1979-03-28
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

U-MAT is the device name listed in this FDA 510(k) record. The listed applicant is Engineering Dynamics Corp.. It received FDA 510(k) clearance on 1979-03-28 under 510(k) number K790466. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the U-MAT?

U-MAT is a medical device that received FDA 510(k) clearance on 1979-03-28. The listed applicant is Engineering Dynamics Corp.. The 510(k) number is K790466.

When did U-MAT receive FDA 510(k) clearance?

U-MAT received FDA 510(k) clearance on 1979-03-28, under 510(k) number K790466.

Who is the listed applicant for U-MAT?

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

What is the FDA product code for U-MAT?

The FDA product code for U-MAT is IYX.

Other records listing Engineering Dynamics Corp. as applicant

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Related Devices (Code: IYX)

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.

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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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