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FDA 510(k)

ARM RADIATION BEAM SCANNER

K-Number: K933558 · 1994-03-16

ApplicantAdvanced Radiation Measurements, Inc.
Decision Date1994-03-16
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARM RADIATION BEAM SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Radiation Measurements, Inc.. It received FDA 510(k) clearance on 1994-03-16 under 510(k) number K933558. 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 ARM RADIATION BEAM SCANNER?

ARM RADIATION BEAM SCANNER is a medical device that received FDA 510(k) clearance on 1994-03-16. The listed applicant is Advanced Radiation Measurements, Inc.. The 510(k) number is K933558.

When did ARM RADIATION BEAM SCANNER receive FDA 510(k) clearance?

ARM RADIATION BEAM SCANNER received FDA 510(k) clearance on 1994-03-16, under 510(k) number K933558.

Who is the listed applicant for ARM RADIATION BEAM SCANNER?

The FDA 510(k) record lists Advanced Radiation Measurements, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARM RADIATION BEAM SCANNER?

The FDA product code for ARM RADIATION BEAM SCANNER is IYE.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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