FDA 510(k) Applications for Medical Device Product Code: LDR (Controller, Infusion, Intravascular, Electronic)

FDA 510(k) Applications for Medical Device Product Code "LDR"
(Controller, Infusion, Intravascular, Electronic)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K971826	ALEXANDER MFG. CO.	ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500	07/03/1997
K971865	ALEXANDER MFG. CO.	ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3P	07/03/1997
K153760	DEKA RESEARCH & DEVELOPMENT	Volumetric Infusion Controller	10/03/2016
K232316	DEKA Research and Development	DEKA Infusion System, DEKA Administration Set	03/01/2024
K242693	DEKA Research and Development Corporation	DEKA Infusion System, DEKA Administration Set	10/07/2024
K963136	HEALTH WATCH, INC.	PACER MODEL 100 INFUSION CONTROLLER	10/10/1997