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Sandhill Scientific, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
16
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K111013ACEMDecember 19, 2011
K012232INSIGHT, MODEL S980000June 7, 2002
K013951SANDHILL SCIENTIFIC PEDIATEC PH PROBEFebruary 28, 2002
K002427SANDHILL UNITIP CATHETER PRESSURE SENSOR, MODEL K 5251-L3-0026June 22, 2001
K990441INSIGHT SPHINCTER OF ODDI MANOMETRY MODULE, MODEL S981300May 12, 1999
K984444INSIGHT GASTROINTESTINAL MOTILITY SYSTEM, MODEL S980000January 11, 1999
K961056BIOVIEW MODEL S960000June 6, 1996
K942247SMALL BOWEL ANALYSIS SOFTWAREApril 9, 1996
K941801ANALGRAPHSeptember 8, 1995
K931963SANDHILL DISPOSABLE INTERNAL REFERENCE PH PROBESeptember 28, 1994
K926218EISMAN-TRIES MEP (MULTIPLE ELECTRODE PROBE)August 26, 1994
K931175SCHUSTER DISPOSABLE BALLOON PROBEApril 1, 1994
K932306MICROINFUSORApril 1, 1994
K912772SUPERLOGGERFebruary 7, 1992
K904231MODEL OSP, SANDHILL AMSJanuary 2, 1991
K834512SANDMILL RMSFebruary 21, 1984