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FDA 510(k)

MULTIPLE PINHOLE TOMOGRAPHIC COLLIMOTER

K-Number: K790499 · 1979-03-26

Decision Date1979-03-26
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTIPLE PINHOLE TOMOGRAPHIC COLLIMOTER 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 1979-03-26 under 510(k) number K790499. 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 MULTIPLE PINHOLE TOMOGRAPHIC COLLIMOTER?

MULTIPLE PINHOLE TOMOGRAPHIC COLLIMOTER is a medical device that received FDA 510(k) clearance on 1979-03-26. The listed applicant is Engineering Dynamics Corp.. The 510(k) number is K790499.

When did MULTIPLE PINHOLE TOMOGRAPHIC COLLIMOTER receive FDA 510(k) clearance?

MULTIPLE PINHOLE TOMOGRAPHIC COLLIMOTER received FDA 510(k) clearance on 1979-03-26, under 510(k) number K790499.

Who is the listed applicant for MULTIPLE PINHOLE TOMOGRAPHIC COLLIMOTER?

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 MULTIPLE PINHOLE TOMOGRAPHIC COLLIMOTER?

The FDA product code for MULTIPLE PINHOLE TOMOGRAPHIC COLLIMOTER is IYX.

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.

View all 10 devices →

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.

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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