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FDA 510(k)

LINEAR ACCELERATOR G-2900

K-Number: K771260 · 1977-08-03

Decision Date1977-08-03
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LINEAR ACCELERATOR G-2900 is the device name listed in this FDA 510(k) record. The listed applicant is Atomic Energy of Canada. It received FDA 510(k) clearance on 1977-08-03 under 510(k) number K771260. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINEAR ACCELERATOR G-2900?

LINEAR ACCELERATOR G-2900 is a medical device that received FDA 510(k) clearance on 1977-08-03. The listed applicant is Atomic Energy of Canada. The 510(k) number is K771260.

When did LINEAR ACCELERATOR G-2900 receive FDA 510(k) clearance?

LINEAR ACCELERATOR G-2900 received FDA 510(k) clearance on 1977-08-03, under 510(k) number K771260.

Who is the listed applicant for LINEAR ACCELERATOR G-2900?

The FDA 510(k) record lists Atomic Energy of Canada as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LINEAR ACCELERATOR G-2900?

The FDA product code for LINEAR ACCELERATOR G-2900 is IYE.

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 Atomic Energy of Canada 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.

Related Devices (Code: IYE)

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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