OXFORD INTENSIVE CARE PATIENT MON. SYS

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 Oxford Intensive Care Patient Mon. Sys.

Pre-market Notification Details

Device IDK802033
510k NumberK802033
Device Name:OXFORD INTENSIVE CARE PATIENT MON. SYS
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 Received1980-08-22
Decision Date1980-09-26

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