FDA 510(k) Applications for Medical Device Product Code: QJY ()

FDA 510(k) Applications for Medical Device Product Code "QJY"

FDA 510(k) Number	Applicant	Device Name	Decision Date
K191313	DEKA Research & Development	Unity Subcutaneous Infusion System for Remodulin	02/21/2020
K243354	DEKA Research & Development Corp.	Remunity System	11/27/2024
K202690	DEKA Research and Development	Remunity Pump for Remodulin (treprostinil) Injection	12/30/2020
K240256	Deka Research and Development	Remunity System	06/12/2024