LINEAR ACCELERATOR G-2900
K-Number: K771260 · 1977-08-03
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Device Summary
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
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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