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FDA 510(k)

MILLENNIUM MLC -120

K-Number: K990085 · 1999-02-08

ApplicantVarian Assoc., Inc.
Decision Date1999-02-08
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MILLENNIUM MLC -120 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 1999-02-08 under 510(k) number K990085. 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 MILLENNIUM MLC -120?

MILLENNIUM MLC -120 is a medical device that received FDA 510(k) clearance on 1999-02-08. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K990085.

When did MILLENNIUM MLC -120 receive FDA 510(k) clearance?

MILLENNIUM MLC -120 received FDA 510(k) clearance on 1999-02-08, under 510(k) number K990085.

Who is the listed applicant for MILLENNIUM MLC -120?

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 MILLENNIUM MLC -120?

The FDA product code for MILLENNIUM MLC -120 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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