FDA 510(k) Applications Submitted by MEDICATECH USA

FDA 510(k) Number	Submission Date	Device Name	Applicant
K080582	03/03/2008	MEDICATECH, MODEL DDR MAK-800, DDT MAK-1000 FS, DDR MAK-1100 FA	MEDICATECH USA
K112132	07/26/2011	KRYSTALRAD 660 DIGITAL RADIOGRAPHIC PORTABLE RETROFIT SYSTEM	MEDICATECH USA
K082798	09/23/2008	DIGITAL DIAGNOSTIC X-RAY SYSTEM, MODELS MAK 1500, MAK 2000 AND MAK 3000	MEDICATECH USA
K130377	02/14/2013	KRYSTALRAD NEW SERIESDIGITAL RADIOGRAPHIC PORTABLE RETROFIT SYSTEM	MEDICATECH USA
K190601	03/08/2019	MasteRad MX30	MedicaTech USA
K230918	04/03/2023	MasterX 800 Series	Medicatech USA
K143257	11/13/2014	KrystalRad 11000 and KrystalRad 3000 Digital Stationary Radiographic System	MEDICATECH USA
K102284	08/12/2010	KRYSTALRAD 560 (FLAATZ 560)	MEDICATECH USA
K102285	08/12/2010	KRYSTALRAD (ATAL8)	MEDICATECH USA