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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