CONMED ECG MONITORING ELECTRODES , MODEL 1700 ( INCLUDING 2500), 1750, 2700, 2710, 1800, SERIES

Electrode, Electrocardiograph

CONMED CORPORATION

The following data is part of a premarket notification filed by Conmed Corporation with the FDA for Conmed Ecg Monitoring Electrodes , Model 1700 ( Including 2500), 1750, 2700, 2710, 1800, Series.

Pre-market Notification Details

Device IDK091856
510k NumberK091856
Device Name:CONMED ECG MONITORING ELECTRODES , MODEL 1700 ( INCLUDING 2500), 1750, 2700, 2710, 1800, SERIES
ClassificationElectrode, Electrocardiograph
Applicant CONMED CORPORATION 525 FRENCH RD. Utica,  NY  13502
ContactSandra Coveleski
CorrespondentSandra Coveleski
CONMED CORPORATION 525 FRENCH RD. Utica,  NY  13502
Product CodeDRX  
CFR Regulation Number870.2360 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2009-06-23
Decision Date2009-08-07
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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