FDA 510(k) Applications Submitted by Aesku Diagnostics GmbH & Co. KG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K172348 | 08/03/2017 | AESKUSLIDES nDNA (Crithidia luciliae), AESKUSLIDES nDNA (Crithidia luciliae) Demo Kit, AESKUSLIDES nDNA (Crithidia luciliae) Bulk kit x5, AESKUSLIDES nDNA (Crithidia luciliae) Bulk kit x10 | Aesku Diagnostics GmbH & Co. KG |
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