FDA 510(k) Applications Submitted by LIVING DATA TECHNOLOGIES CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K023701 | 11/04/2002 | ANGIONEW-IV | LIVING DATA TECHNOLOGIES CORPORATION |
| K033657 | 11/21/2003 | MOBILE EXTERNAL COUNTER PULSATION SYSTEM ANGIONEW-V | LIVING DATA TECHNOLOGIES CORPORATION |
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