SyMRI

System, Nuclear Magnetic Resonance Imaging

SyntheticMR AB

The following data is part of a premarket notification filed by Syntheticmr Ab with the FDA for Symri.

Pre-market Notification Details

Device IDK203372
510k NumberK203372
Device Name:SyMRI
ClassificationSystem, Nuclear Magnetic Resonance Imaging
Applicant SyntheticMR AB Storgatan 11 Linkoping,  SE 582 23
ContactLisa Warnroth
CorrespondentRaymond Kelly
Licensale Inc 3422 Leonardo Lane New Smyrna Lane,  FL  32168
Product CodeLNH  
CFR Regulation Number892.1000 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2020-11-16
Decision Date2021-11-03

Trademark Results [SyMRI]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SYMRI
SYMRI
85974094 4661808 Live/Registered
Synthetic MR AB (publ)
2013-07-01

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