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FDA 510(k)

DOSIMETRY CHECK

K-Number: K010225 · 2001-04-24

ApplicantMath Resolutions, LLC
Decision Date2001-04-24
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DOSIMETRY CHECK is the device name listed in this FDA 510(k) record. The listed applicant is Math Resolutions, LLC. It received FDA 510(k) clearance on 2001-04-24 under 510(k) number K010225. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOSIMETRY CHECK?

DOSIMETRY CHECK is a medical device that received FDA 510(k) clearance on 2001-04-24. The listed applicant is Math Resolutions, LLC. The 510(k) number is K010225.

When did DOSIMETRY CHECK receive FDA 510(k) clearance?

DOSIMETRY CHECK received FDA 510(k) clearance on 2001-04-24, under 510(k) number K010225.

Who is the listed applicant for DOSIMETRY CHECK?

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

What is the FDA product code for DOSIMETRY CHECK?

The FDA product code for DOSIMETRY CHECK is IYE.

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Other records listing Math Resolutions, LLC 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.

K162577Dosimetry Check Version 5 Release 1K132605DOSIMETRY CHECK VERSION 4 RELEASE 1K101503DUSIMETRY CHECKK050372VISITRAK, VERSION 1, RELEASE 1K022961RTDOSEPLANK011845MILLCOMP

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Related Devices (Code: IYE)

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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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