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FDA 510(k)

CLINAC 20

K-Number: K771358 · 1977-08-16

ApplicantVarian Assoc., Inc.
Decision Date1977-08-16
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CLINAC 20 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 1977-08-16 under 510(k) number K771358. 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 CLINAC 20?

CLINAC 20 is a medical device that received FDA 510(k) clearance on 1977-08-16. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K771358.

When did CLINAC 20 receive FDA 510(k) clearance?

CLINAC 20 received FDA 510(k) clearance on 1977-08-16, under 510(k) number K771358.

Who is the listed applicant for CLINAC 20?

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 CLINAC 20?

The FDA product code for CLINAC 20 is IYE.

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Other records listing Varian Assoc., Inc. as applicant

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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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