Interson Corp. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Interson Corp. has 9 FDA 510(k) cleared medical devices. Based in Pleasanton, US.
Historical record: 9 cleared submissions from 1989 to 1991. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Interson Corp. Filter by specialty or product code using the sidebar.
9 devices
Cleared
Dec 20, 1991
INTERSON ENDOCAVITY PROBE/KONTRON ULTRASOUND SYST
Radiology
288d
Cleared
Dec 17, 1991
INTERSON TRANSRECTAL PROBE/KONTRON ULTRASOUND SYST
Radiology
285d
Cleared
Dec 17, 1991
INTERSON TRANSRECTAL PROBE/ATL ULTRASOUND SYSTEM
Radiology
285d
Cleared
Dec 17, 1991
INTERSON ENDOCAVITY PROBE FOR ATL ULTRASOUND SYST
Radiology
285d
Cleared
Nov 19, 1991
INTERSON ENDOCAVITY PROBE/ALOKA ULTRASOUND SYSTEM
Radiology
257d
Cleared
Sep 27, 1991
INTERSON DISPOSABLE BIOPSY NEEDLE
Radiology
177d
Cleared
May 02, 1990
INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA.
Radiology
85d
Cleared
Feb 14, 1990
PROBE SHEATH FOR ADMS & CAPISTRANO LABS TRANSREC.
Gastroenterology & Urology
79d
Cleared
Nov 06, 1989
BIOPSY NEEDLE GUIDE FOR ADMS ULTRASOUND PROBES
Gastroenterology & Urology
42d