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FDA 510(k)

VARIAN C-SERIES CLINACS (CLINAC 2300C/D)

K-Number: K913119 · 1991-11-07

ApplicantVarian Assoc., Inc.
Decision Date1991-11-07
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARIAN C-SERIES CLINACS (CLINAC 2300C/D) 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 1991-11-07 under 510(k) number K913119. 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 2300C/D)?

VARIAN C-SERIES CLINACS (CLINAC 2300C/D) is a medical device that received FDA 510(k) clearance on 1991-11-07. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K913119.

When did VARIAN C-SERIES CLINACS (CLINAC 2300C/D) receive FDA 510(k) clearance?

VARIAN C-SERIES CLINACS (CLINAC 2300C/D) received FDA 510(k) clearance on 1991-11-07, under 510(k) number K913119.

Who is the listed applicant for VARIAN C-SERIES CLINACS (CLINAC 2300C/D)?

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 2300C/D)?

The FDA product code for VARIAN C-SERIES CLINACS (CLINAC 2300C/D) 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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