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FDA 510(k)

VARIAN MULTILEAF COLLIMATOR

K-Number: K893464 · 1989-08-10

ApplicantVarian Assoc., Inc.
Decision Date1989-08-10
Product CodeIXI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARIAN MULTILEAF COLLIMATOR 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 1989-08-10 under 510(k) number K893464. The device is classified under product code IXI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARIAN MULTILEAF COLLIMATOR?

VARIAN MULTILEAF COLLIMATOR is a medical device that received FDA 510(k) clearance on 1989-08-10. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K893464.

When did VARIAN MULTILEAF COLLIMATOR receive FDA 510(k) clearance?

VARIAN MULTILEAF COLLIMATOR received FDA 510(k) clearance on 1989-08-10, under 510(k) number K893464.

Who is the listed applicant for VARIAN MULTILEAF COLLIMATOR?

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 MULTILEAF COLLIMATOR?

The FDA product code for VARIAN MULTILEAF COLLIMATOR is IXI.

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Other records listing Varian Assoc., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K000922PROTON VISIONK992762BRACHYVISION 6.0K992751SOMAVISIONK992753CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEMK990085MILLENNIUM MLC -120K980601VARISOURCE WRIGHT VAGINAL CUFF APPLICATOR FOR VARIAN VARISOURCE REMOTE HIGH DOSE RATE AFTERIOADER

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Related Devices (Code: IXI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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