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FDA 510(k)

PREFERNCE IMRT TREATMENT PLANNING MODULE

K-Number: K012575 · 2002-03-12

Decision Date2002-03-12
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PREFERNCE IMRT TREATMENT PLANNING MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Northwest Medical Physics Equipment, Inc.. It received FDA 510(k) clearance on 2002-03-12 under 510(k) number K012575. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PREFERNCE IMRT TREATMENT PLANNING MODULE?

PREFERNCE IMRT TREATMENT PLANNING MODULE is a medical device that received FDA 510(k) clearance on 2002-03-12. The listed applicant is Northwest Medical Physics Equipment, Inc.. The 510(k) number is K012575.

When did PREFERNCE IMRT TREATMENT PLANNING MODULE receive FDA 510(k) clearance?

PREFERNCE IMRT TREATMENT PLANNING MODULE received FDA 510(k) clearance on 2002-03-12, under 510(k) number K012575.

Who is the listed applicant for PREFERNCE IMRT TREATMENT PLANNING MODULE?

The FDA 510(k) record lists Northwest Medical Physics Equipment, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PREFERNCE IMRT TREATMENT PLANNING MODULE?

The FDA product code for PREFERNCE IMRT TREATMENT PLANNING MODULE is MUJ.

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.

Other records listing Northwest Medical Physics Equipment, Inc. 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.

Related Devices (Code: MUJ)

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.

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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