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FDA 510(k)

RADIOTHERAPY MGMT. SYSTEM RMS-1000

K-Number: K832732 · 1983-09-29

ApplicantVarian Assoc., Inc.
Decision Date1983-09-29
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADIOTHERAPY MGMT. SYSTEM RMS-1000 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 1983-09-29 under 510(k) number K832732. 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 RADIOTHERAPY MGMT. SYSTEM RMS-1000?

RADIOTHERAPY MGMT. SYSTEM RMS-1000 is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K832732.

When did RADIOTHERAPY MGMT. SYSTEM RMS-1000 receive FDA 510(k) clearance?

RADIOTHERAPY MGMT. SYSTEM RMS-1000 received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832732.

Who is the listed applicant for RADIOTHERAPY MGMT. SYSTEM RMS-1000?

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 RADIOTHERAPY MGMT. SYSTEM RMS-1000?

The FDA product code for RADIOTHERAPY MGMT. SYSTEM RMS-1000 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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