Inrad - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
FDA 510(k) Regulatory Record - Inrad Gastroenterology & Urology ✕
6 devices
Cleared
Nov 19, 2009
PRECISECORE 10 MM BIOPSY DEVICE- 14GA X 5 CM MODEL 670514, 671014, 670518...
Gastroenterology & Urology
17d
Cleared
Nov 17, 2009
SELECTCORE VARIABLE THROW BIOPSY DEVICE MODEL 991014, 991514, 991018, 991518,...
Gastroenterology & Urology
29d
Cleared
Jun 04, 2009
REVOLUTION FULL CORE BIOPSY
Gastroenterology & Urology
90d
Cleared
Apr 24, 2000
ACCUCORE SINGLE ACTION CORE BIOPSY DEVICE
Gastroenterology & Urology
61d
Cleared
Jul 28, 1998
C0-AXIAL INTRODUCER NEEDLE
Gastroenterology & Urology
74d
Cleared
Jun 22, 1998
ACCUCORE CORE BIOPSY NEEDLE CATALOG CODES:581014, 581614, 581618, 582018,...
Gastroenterology & Urology
83d