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FDA 510(k)

DOSE VOLUME HISTOGRAM (DVH) EVALUATOR

K-Number: K092928 · 2009-12-16

ApplicantDiversilabs, LLC
Decision Date2009-12-16
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DOSE VOLUME HISTOGRAM (DVH) EVALUATOR is the device name listed in this FDA 510(k) record. The listed applicant is Diversilabs, LLC. It received FDA 510(k) clearance on 2009-12-16 under 510(k) number K092928. 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 DOSE VOLUME HISTOGRAM (DVH) EVALUATOR?

DOSE VOLUME HISTOGRAM (DVH) EVALUATOR is a medical device that received FDA 510(k) clearance on 2009-12-16. The listed applicant is Diversilabs, LLC. The 510(k) number is K092928.

When did DOSE VOLUME HISTOGRAM (DVH) EVALUATOR receive FDA 510(k) clearance?

DOSE VOLUME HISTOGRAM (DVH) EVALUATOR received FDA 510(k) clearance on 2009-12-16, under 510(k) number K092928.

Who is the listed applicant for DOSE VOLUME HISTOGRAM (DVH) EVALUATOR?

The FDA 510(k) record lists Diversilabs, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DOSE VOLUME HISTOGRAM (DVH) EVALUATOR?

The FDA product code for DOSE VOLUME HISTOGRAM (DVH) EVALUATOR is MUJ.

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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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