Inrad is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Inrad - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Inrad has 11 FDA 510(k) cleared medical devices. Based in Kentwood, US.
Historical record: 11 cleared submissions from 1998 to 2009. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Inrad Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Inrad
11 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
Jan 30, 2007
ULTRACLIP II WING AND ULTRACLIP II COIL
General & Plastic Surgery
96d
Cleared
Sep 20, 2004
ULTRACLIP II US
General & Plastic Surgery
21d
Cleared
Jun 03, 2004
ULTRACLIP II MR
General & Plastic Surgery
27d
Cleared
Apr 24, 2000
ACCUCORE SINGLE ACTION CORE BIOPSY DEVICE
Gastroenterology & Urology
61d
Cleared
Feb 04, 2000
ULTRACLIP TISSUE MARKER
General & Plastic Surgery
88d
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
Cleared
Apr 17, 1998
IV DECANTER-FLEXIBLE
General Hospital
59d