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FDA 510(k)

VARIAN MULTILEAF COLLIMATOR WITH DYNAMIC ARC THERAPY FEATURE

K-Number: K973889 · 1997-11-21

ApplicantVarian Medical Systems, Inc.
Decision Date1997-11-21
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARIAN MULTILEAF COLLIMATOR WITH DYNAMIC ARC THERAPY FEATURE is the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 1997-11-21 under 510(k) number K973889. 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 MULTILEAF COLLIMATOR WITH DYNAMIC ARC THERAPY FEATURE?

VARIAN MULTILEAF COLLIMATOR WITH DYNAMIC ARC THERAPY FEATURE is a medical device that received FDA 510(k) clearance on 1997-11-21. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K973889.

When did VARIAN MULTILEAF COLLIMATOR WITH DYNAMIC ARC THERAPY FEATURE receive FDA 510(k) clearance?

VARIAN MULTILEAF COLLIMATOR WITH DYNAMIC ARC THERAPY FEATURE received FDA 510(k) clearance on 1997-11-21, under 510(k) number K973889.

Who is the listed applicant for VARIAN MULTILEAF COLLIMATOR WITH DYNAMIC ARC THERAPY FEATURE?

The FDA 510(k) record lists Varian Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VARIAN MULTILEAF COLLIMATOR WITH DYNAMIC ARC THERAPY FEATURE?

The FDA product code for VARIAN MULTILEAF COLLIMATOR WITH DYNAMIC ARC THERAPY FEATURE 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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