FDA 510(k) Applications Submitted by ALIVE, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K980892 | 03/09/1998 | HAKOMED ELECDT / PRO ELEDT SERIES | ALIVE, INC. |
| K980958 | 03/16/1998 | HAKOMED ELECDT/VACUPULLS | ALIVE, INC. |
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