ANALYZER, MEDILOG II

Detector And Alarm, Arrhythmia

OXFORD MEDILOG, INC.

The following data is part of a premarket notification filed by Oxford Medilog, Inc. with the FDA for Analyzer, Medilog Ii.

Pre-market Notification Details

Device IDK790287
510k NumberK790287
Device Name:ANALYZER, MEDILOG II
ClassificationDetector And Alarm, Arrhythmia
Applicant OXFORD MEDILOG, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeDSI  
CFR Regulation Number870.1025 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1979-02-08
Decision Date1979-02-28

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