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FDA 510(k)

VARIAN RMS-2000, RELEASE 2.5

K-Number: K930513 · 1994-09-23

ApplicantVarian Assoc., Inc.
Decision Date1994-09-23
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARIAN RMS-2000, RELEASE 2.5 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 1994-09-23 under 510(k) number K930513. 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 RMS-2000, RELEASE 2.5?

VARIAN RMS-2000, RELEASE 2.5 is a medical device that received FDA 510(k) clearance on 1994-09-23. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K930513.

When did VARIAN RMS-2000, RELEASE 2.5 receive FDA 510(k) clearance?

VARIAN RMS-2000, RELEASE 2.5 received FDA 510(k) clearance on 1994-09-23, under 510(k) number K930513.

Who is the listed applicant for VARIAN RMS-2000, RELEASE 2.5?

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 RMS-2000, RELEASE 2.5?

The FDA product code for VARIAN RMS-2000, RELEASE 2.5 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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