Dymax Corp - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Dymax Corp has 7 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.
Historical record: 7 cleared submissions from 1985 to 2003. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Dymax Corp Filter by specialty or product code using the sidebar.
7 devices
Cleared
Jul 21, 2003
SITE-RITE IV ULTRASOUND SYSTEM
Radiology
10d
Cleared
Nov 10, 1999
SITE-RITE 3 ULTRASOUND SYSTEM
Radiology
15d
Cleared
Jul 27, 1993
SITERITE NEEDLE GUIDE (MODIFIED)
Cardiovascular
130d
Cleared
Sep 27, 1990
SITERITE NEEDLE GUIDE
Cardiovascular
71d
Cleared
Oct 25, 1989
DYMAX ENDOVAGINAL BIOPSY GUIDE
Obstetrics & Gynecology
100d
Cleared
Dec 11, 1986
DYMAX PERSONAL SCANNER
Radiology
190d
Cleared
Apr 15, 1985
PLUS 1
Radiology
63d