FDA 510(k) Applications Submitted by CORTEX BIOPHYSIK GMBH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K001631 | 05/26/2000 | CORTEX METAMAX | CORTEX BIOPHYSIK GMBH |
| K993641 | 10/28/1999 | METALYZER, MODEL 2; METALYZER, MODEL 3 | CORTEX BIOPHYSIK GMBH |
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