MT-200

Computer, Diagnostic, Programmable

SCHILLER AMERICA, INC.

The following data is part of a premarket notification filed by Schiller America, Inc. with the FDA for Mt-200.

Pre-market Notification Details

Device IDK973751
510k NumberK973751
Device Name:MT-200
ClassificationComputer, Diagnostic, Programmable
Applicant SCHILLER AMERICA, INC. 3002 DOW AVE., #138 Tustin,  CA  92780
ContactMarkus Maritz
CorrespondentMarkus Maritz
SCHILLER AMERICA, INC. 3002 DOW AVE., #138 Tustin,  CA  92780
Product CodeDQK  
CFR Regulation Number870.1425 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1997-10-01
Decision Date1998-08-25
Summary:summary

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