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FDA 510(k)

GENERAL ULTRASOUND EXAM. TABLE

K-Number: K802254 · 1980-11-26

Decision Date1980-11-26
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GENERAL ULTRASOUND EXAM. TABLE 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 1980-11-26 under 510(k) number K802254. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENERAL ULTRASOUND EXAM. TABLE?

GENERAL ULTRASOUND EXAM. TABLE is a medical device that received FDA 510(k) clearance on 1980-11-26. The listed applicant is Engineering Dynamics Corp.. The 510(k) number is K802254.

When did GENERAL ULTRASOUND EXAM. TABLE receive FDA 510(k) clearance?

GENERAL ULTRASOUND EXAM. TABLE received FDA 510(k) clearance on 1980-11-26, under 510(k) number K802254.

Who is the listed applicant for GENERAL ULTRASOUND EXAM. TABLE?

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 GENERAL ULTRASOUND EXAM. TABLE?

The FDA product code for GENERAL ULTRASOUND EXAM. TABLE is IYN.

Related Clinical Trials

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.

Other records listing Engineering Dynamics Corp. 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.

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Related Devices (Code: IYN)

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.

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.

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