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Neoprobe Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K050088QUANTIX/OR BLOOD FLOW MONITOR; FLEXIBLE PROBE WITH OPTIONAL VESSEL STABILIZERFebruary 8, 2005
K971167NEOPROBE MODEL 1500 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIESJune 26, 1997
K962319NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIESSeptember 13, 1996
K942580NEOPROBE 1000 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIESFebruary 9, 1995
K915279NEOPROBE PORTABLE RADIOSCOPE DETECTORJune 10, 1992
K864263NEOPROBE PORTABLE RADIOISOTOPE DETECTORDecember 29, 1986