DOSIMETRY CHECK

Accelerator, Linear, Medical

MATH RESOLUTIONS, LLC.

The following data is part of a premarket notification filed by Math Resolutions, Llc. with the FDA for Dosimetry Check.

Pre-market Notification Details

Device IDK010225
510k NumberK010225
Device Name:DOSIMETRY CHECK
ClassificationAccelerator, Linear, Medical
Applicant MATH RESOLUTIONS, LLC. 5975 GALES LN. Columbia,  MD  21045
ContactWendel D Renner
CorrespondentWendel D Renner
MATH RESOLUTIONS, LLC. 5975 GALES LN. Columbia,  MD  21045
Product CodeIYE  
CFR Regulation Number892.5050 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2001-01-24
Decision Date2001-04-24

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
B229DC051 K010225 000
B229DC041 K010225 000

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