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FDA 510(k)

CLINAC 12/10

K-Number: K781174 · 1978-09-14

ApplicantVarian Assoc., Inc.
Decision Date1978-09-14
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CLINAC 12/10 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 1978-09-14 under 510(k) number K781174. 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 12/10?

CLINAC 12/10 is a medical device that received FDA 510(k) clearance on 1978-09-14. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K781174.

When did CLINAC 12/10 receive FDA 510(k) clearance?

CLINAC 12/10 received FDA 510(k) clearance on 1978-09-14, under 510(k) number K781174.

Who is the listed applicant for CLINAC 12/10?

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 12/10?

The FDA product code for CLINAC 12/10 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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