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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