Medicatech USA
Medicatech USA holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2023.
Top product codes for Medicatech USA
Recent clearances by Medicatech USA
- K230918 — MasterX 800 Series
- K190601 — MasteRad MX30
- K143257 — KrystalRad 11000 and KrystalRad 3000 Digital Stationary Radiographic System
- K130377 — KRYSTALRAD NEW SERIESDIGITAL RADIOGRAPHIC PORTABLE RETROFIT SYSTEM
- K112132 — KRYSTALRAD 660 DIGITAL RADIOGRAPHIC PORTABLE RETROFIT SYSTEM
- K102284 — KRYSTALRAD 560 (FLAATZ 560)
- K102285 — KRYSTALRAD (ATAL8)
- K082798 — DIGITAL DIAGNOSTIC X-RAY SYSTEM, MODELS MAK 1500, MAK 2000 AND MAK 3000
- K080582 — MEDICATECH, MODEL DDR MAK-800, DDT MAK-1000 FS, DDR MAK-1100 FA
Data sourced from openFDA. This site is unofficial and independent of the FDA.