MEVACHECK

Accelerator, Linear, Medical

MAGUS MICROCONTROLLERS, INC.

The following data is part of a premarket notification filed by Magus Microcontrollers, Inc. with the FDA for Mevacheck.

Pre-market Notification Details

Device IDK864910
510k NumberK864910
Device Name:MEVACHECK
ClassificationAccelerator, Linear, Medical
Applicant MAGUS MICROCONTROLLERS, INC. 4252 COMMERCE CIRCLE VICTORIA, B.C. Canada V8z4mz,  CA
ContactMorris, Phd
CorrespondentMorris, Phd
MAGUS MICROCONTROLLERS, INC. 4252 COMMERCE CIRCLE VICTORIA, B.C. Canada V8z4mz,  CA
Product CodeIYE  
CFR Regulation Number892.5050 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1986-12-15
Decision Date1987-03-16

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