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FDA 510(k)

ELECTRON ARC THERAPY

K-Number: K802809 · 1981-01-07

ApplicantVarian Assoc., Inc.
Decision Date1981-01-07
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ELECTRON ARC THERAPY is the device name listed in this FDA 510(k) record. The listed applicant is Varian Assoc., Inc.. It received FDA 510(k) clearance on 1981-01-07 under 510(k) number K802809. 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 ELECTRON ARC THERAPY?

ELECTRON ARC THERAPY is a medical device that received FDA 510(k) clearance on 1981-01-07. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K802809.

When did ELECTRON ARC THERAPY receive FDA 510(k) clearance?

ELECTRON ARC THERAPY received FDA 510(k) clearance on 1981-01-07, under 510(k) number K802809.

Who is the listed applicant for ELECTRON ARC THERAPY?

The FDA 510(k) record lists Varian Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRON ARC THERAPY?

The FDA product code for ELECTRON ARC THERAPY is IYE.

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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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