FDA 510(k) Applications Submitted by DiaSys Diagnostic Systems GmbH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K242294 | 08/02/2024 | DiaSys Procalcitonin FS; DiaSys TruCal Procalcitonin Calibrator Set; DiaSys TruLab Procalcitonin Bi-Level Controls | DiaSys Diagnostic Systems GmbH |
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