Sandhill Scientific, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sandhill Scientific, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Sandhill Scientific, Inc. has 16 FDA 510(k) cleared gastroenterology & urology devices. Based in Mchenry, US.
Historical record: 16 cleared submissions from 1984 to 2011.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sandhill Scientific, Inc.
16 devices
Cleared
Dec 19, 2011
ACEM
Gastroenterology & Urology
252d
Cleared
Jun 07, 2002
INSIGHT, MODEL S980000
Gastroenterology & Urology
326d
Cleared
Feb 28, 2002
SANDHILL SCIENTIFIC PEDIATEC PH PROBE
Gastroenterology & Urology
90d
Cleared
Jun 22, 2001
SANDHILL UNITIP CATHETER PRESSURE SENSOR, MODEL K 5251-L3-0026
Gastroenterology & Urology
318d
Cleared
May 12, 1999
INSIGHT SPHINCTER OF ODDI MANOMETRY MODULE, MODEL S981300
Gastroenterology & Urology
90d
Cleared
Jan 11, 1999
INSIGHT GASTROINTESTINAL MOTILITY SYSTEM, MODEL S980000
Gastroenterology & Urology
28d
Cleared
Jun 06, 1996
BIOVIEW MODEL S960000
Gastroenterology & Urology
80d
Cleared
Apr 09, 1996
SMALL BOWEL ANALYSIS SOFTWARE
Gastroenterology & Urology
701d
Cleared
Sep 08, 1995
ANALGRAPH
Gastroenterology & Urology
514d
Cleared
Sep 28, 1994
SANDHILL DISPOSABLE INTERNAL REFERENCE PH PROBE
Gastroenterology & Urology
525d
Cleared
Aug 26, 1994
EISMAN-TRIES MEP (MULTIPLE ELECTRODE PROBE)
Gastroenterology & Urology
624d
Cleared
Apr 01, 1994
SCHUSTER DISPOSABLE BALLOON PROBE
Gastroenterology & Urology
388d