LME TEMP. MONITOR

Thermometer, Electronic, Clinical

LITTON MEDICAL ELECTRONICS

The following data is part of a premarket notification filed by Litton Medical Electronics with the FDA for Lme Temp. Monitor.

Pre-market Notification Details

Device IDK832042
510k NumberK832042
Device Name:LME TEMP. MONITOR
ClassificationThermometer, Electronic, Clinical
Applicant LITTON MEDICAL ELECTRONICS 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeFLL  
CFR Regulation Number880.2910 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-06-24
Decision Date1983-08-12

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