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FDA 510(k)

ARS-1000 RADIATION THERAPY TREATMENT PLANNING SYSTEM

K-Number: K827175 · 1982-03-31

ApplicantApplied Radiation
Decision Date1982-03-31
Product Code
DecisionSubstantially Equivalent

Device Summary

ARS-1000 RADIATION THERAPY TREATMENT PLANNING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Applied Radiation. It received FDA 510(k) clearance on 1982-03-31 under 510(k) number K827175. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARS-1000 RADIATION THERAPY TREATMENT PLANNING SYSTEM?

ARS-1000 RADIATION THERAPY TREATMENT PLANNING SYSTEM is a medical device that received FDA 510(k) clearance on 1982-03-31. The listed applicant is Applied Radiation. The 510(k) number is K827175.

When did ARS-1000 RADIATION THERAPY TREATMENT PLANNING SYSTEM receive FDA 510(k) clearance?

ARS-1000 RADIATION THERAPY TREATMENT PLANNING SYSTEM received FDA 510(k) clearance on 1982-03-31, under 510(k) number K827175.

Who is the listed applicant for ARS-1000 RADIATION THERAPY TREATMENT PLANNING SYSTEM?

The FDA 510(k) record lists Applied Radiation 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 Applied Radiation 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.

K820448ARS-1000

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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