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FDA 510(k)

VARIAN C-SERIES CLINACS CLINAC 600C,2100C,2500C

K-Number: K904364 · 1991-02-27

ApplicantVarian Assoc., Inc.
Decision Date1991-02-27
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARIAN C-SERIES CLINACS CLINAC 600C,2100C,2500C 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 1991-02-27 under 510(k) number K904364. 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 C-SERIES CLINACS CLINAC 600C,2100C,2500C?

VARIAN C-SERIES CLINACS CLINAC 600C,2100C,2500C is a medical device that received FDA 510(k) clearance on 1991-02-27. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K904364.

When did VARIAN C-SERIES CLINACS CLINAC 600C,2100C,2500C receive FDA 510(k) clearance?

VARIAN C-SERIES CLINACS CLINAC 600C,2100C,2500C received FDA 510(k) clearance on 1991-02-27, under 510(k) number K904364.

Who is the listed applicant for VARIAN C-SERIES CLINACS CLINAC 600C,2100C,2500C?

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 C-SERIES CLINACS CLINAC 600C,2100C,2500C?

The FDA product code for VARIAN C-SERIES CLINACS CLINAC 600C,2100C,2500C 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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