FDA 510(k) Applications Submitted by CORTEX TECHNOLOGY APS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K983945 | 11/05/1998 | CORTEX DERMASCAN C ULTRASONIC SYSTEM | CORTEX TECHNOLOGY APS |
| K982280 | 06/30/1998 | CRYOPRO MAXI AND CRYOPRO MINI | CORTEX TECHNOLOGY APS |
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