FDA 510(k) Applications Submitted by AMLUCK, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K012796 | 08/21/2001 | AMLUCK AUTOMATIC DIGITAL WRIST, BLOOD PRESSURE MONITOR AK-3000/AK-4000 | AMLUCK, INC. |
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