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FDA 510(k)

VARIAN RMS-2000

K-Number: K863358 · 1986-09-19

ApplicantVarian Assoc., Inc.
Decision Date1986-09-19
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARIAN RMS-2000 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 1986-09-19 under 510(k) number K863358. 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?

VARIAN RMS-2000 is a medical device that received FDA 510(k) clearance on 1986-09-19. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K863358.

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

VARIAN RMS-2000 received FDA 510(k) clearance on 1986-09-19, under 510(k) number K863358.

Who is the listed applicant for VARIAN RMS-2000?

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?

The FDA product code for VARIAN RMS-2000 is IYE.

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Other records listing Varian Assoc., Inc. as applicant

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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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