FDA 510(k) Applications for Medical Device Product Code: JEH (Plethysmograph, Volume)

FDA 510(k) Applications for Medical Device Product Code "JEH"
(Plethysmograph, Volume)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K960840	C.E. DIAGNOSIS, INC.	C.E. VASCULAR MACHINE	03/28/1997
K240706	GANSHORN Medizin Electronic GmbH	PowerCube+ Series (PowerCube Body+); PowerCube+ Series (PowerCube Diffusion+); PowerCube+ Series (PowerCube Body+ / Diffusion+)	12/09/2024
K022636	MORGAN SCIENTIFIC, INC.	BODY BOX 5500	01/13/2003
K072061	VIASYS HEALTHCARE GMBH	MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODY	04/22/2008
K223818	Vitalograph Ireland Ltd.	Model 9160 VitaloQUB	05/25/2023