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FDA 510(k) Applications Submitted by DR. LEE CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K972587
07/11/1997
ELECTROCARDIOGRAPHS
DR. LEE CO., LTD.
K972603
07/11/1997
ELECTROCARDIOGRAPHS MODELS 110B, 120B AND 310B
DR. LEE CO., LTD.
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