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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
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