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FDA 510(k)

VERASUN RADIATION THERAPY SIMULATION SYSTEM

K-Number: K837336 · 1983-04-29

ApplicantCgr Medical Corp.
Decision Date1983-04-29
Product Code
DecisionSubstantially Equivalent

Device Summary

VERASUN RADIATION THERAPY SIMULATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cgr Medical Corp.. It received FDA 510(k) clearance on 1983-04-29 under 510(k) number K837336. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERASUN RADIATION THERAPY SIMULATION SYSTEM?

VERASUN RADIATION THERAPY SIMULATION SYSTEM is a medical device that received FDA 510(k) clearance on 1983-04-29. The listed applicant is Cgr Medical Corp.. The 510(k) number is K837336.

When did VERASUN RADIATION THERAPY SIMULATION SYSTEM receive FDA 510(k) clearance?

VERASUN RADIATION THERAPY SIMULATION SYSTEM received FDA 510(k) clearance on 1983-04-29, under 510(k) number K837336.

Who is the listed applicant for VERASUN RADIATION THERAPY SIMULATION SYSTEM?

The FDA 510(k) record lists Cgr Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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.

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Other records listing Cgr Medical Corp. as applicant

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.

K843926PRESTILIX 1690K843235STENOSCOPK843985SUSPENSION 7K841649MAXIMAX - 4K833223SONEL 3000AK833941ORION

View all 20 devices →

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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