MULTISCRIPTOR EK 36/101 047 02,05

Electrocardiograph

LITTON MEDICAL ELECTRONICS

The following data is part of a premarket notification filed by Litton Medical Electronics with the FDA for Multiscriptor Ek 36/101 047 02,05.

Pre-market Notification Details

Device IDK832130
510k NumberK832130
Device Name:MULTISCRIPTOR EK 36/101 047 02,05
ClassificationElectrocardiograph
Applicant LITTON MEDICAL ELECTRONICS 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeDPS  
CFR Regulation Number870.2340 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-07-01
Decision Date1983-10-31

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