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FDA 510(k)

CRS RADIATION BEAM SCANNER

K-Number: K914821 · 1992-12-17

ApplicantConsolidated Radiation Services, Inc.
Decision Date1992-12-17
Product CodeIYI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CRS RADIATION BEAM SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Consolidated Radiation Services, Inc.. It received FDA 510(k) clearance on 1992-12-17 under 510(k) number K914821. The device is classified under product code IYI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRS RADIATION BEAM SCANNER?

CRS RADIATION BEAM SCANNER is a medical device that received FDA 510(k) clearance on 1992-12-17. The listed applicant is Consolidated Radiation Services, Inc.. The 510(k) number is K914821.

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

CRS RADIATION BEAM SCANNER received FDA 510(k) clearance on 1992-12-17, under 510(k) number K914821.

Who is the listed applicant for CRS RADIATION BEAM SCANNER?

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

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

The FDA product code for CRS RADIATION BEAM SCANNER is IYI.

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Related Devices (Code: IYI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K90093237-702 AND 37-703 PC RAINBOWVictoreen, Inc.

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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