FDA 510(k) Applications Submitted by DEKA Research & Development
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K190182 | 02/01/2019 | Unity Subcutaneous Delivery System for Remodulin | DEKA Research & Development |
| K191313 | 05/15/2019 | Unity Subcutaneous Infusion System for Remodulin | DEKA Research & Development |
| K153760 | 12/30/2015 | Volumetric Infusion Controller | DEKA RESEARCH & DEVELOPMENT |
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