WaterProof PROFILER

Accelerator, Linear, Medical

SUN NUCLEAR CORPORATION

The following data is part of a premarket notification filed by Sun Nuclear Corporation with the FDA for Waterproof Profiler.

Pre-market Notification Details

Device IDK142431
510k NumberK142431
Device Name:WaterProof PROFILER
ClassificationAccelerator, Linear, Medical
Applicant SUN NUCLEAR CORPORATION 3275 SUNTREE BOULEVARD Melbourne,  FL  32940
ContactNoel Downey
CorrespondentNoel Downey
SUN NUCLEAR CORPORATION 3275 SUNTREE BOULEVARD Melbourne,  FL  32940
Product CodeIYE  
CFR Regulation Number892.5050 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2014-08-29
Decision Date2014-12-05
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
B01612300009Z0 K142431 000

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