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FDA 510(k) Applications Submitted by EIKON HEALTHCARE DEVICE CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K021239
04/18/2002
EIKON AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-400M
EIKON HEALTHCARE DEVICE CORP.
K021240
04/18/2002
EIKON AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-200M/HD-200
EIKON HEALTHCARE DEVICE CORP.
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