Medical Device Manufacturer · US , Natick , MA

Direx Systems Corp. - FDA 510(k) Cleared Devices

22 submissions · 22 cleared · Since 2003

Total

Cleared

Denied

Direx Systems Corp. has 22 FDA 510(k) cleared medical devices. Based in Natick, US.

Historical record: 22 cleared submissions from 2003 to 2012. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Direx Systems Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Direx Systems Corp.

22 devices

1-12 of 22

Cleared Mar 01, 2012

DUET MAGNA

K111947 · LNS

Gastroenterology & Urology · 237d

CROSSPLAN / ACCUSOFT-XL V.4.04

Gastroenterology & Urology · 85d

Cleared Oct 05, 2006

ACCUSOFT, ACCUSOFT XL

Gastroenterology & Urology · 61d

Direx Systems Corp. - FDA 510(k) Cleared Devices

Filters