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FDA 510(k)

VARIAN CLINAC 600SR

K-Number: K913174 · 1991-11-05

ApplicantVarian Assoc., Inc.
Decision Date1991-11-05
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARIAN CLINAC 600SR 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 1991-11-05 under 510(k) number K913174. 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 VARIAN CLINAC 600SR?

VARIAN CLINAC 600SR is a medical device that received FDA 510(k) clearance on 1991-11-05. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K913174.

When did VARIAN CLINAC 600SR receive FDA 510(k) clearance?

VARIAN CLINAC 600SR received FDA 510(k) clearance on 1991-11-05, under 510(k) number K913174.

Who is the listed applicant for VARIAN CLINAC 600SR?

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 VARIAN CLINAC 600SR?

The FDA product code for VARIAN CLINAC 600SR is IYE.

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Other records listing Varian Assoc., Inc. 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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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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