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Grieshaber & Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K950056THE GRIESHABER AXIAL CUTTERMay 5, 1995
K930842THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGEMay 3, 1994
K914588GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGEJune 11, 1992
K914587GRIESHABER AIR/FLUID TUBING SETJanuary 23, 1992
K914586GRIESHABER THREE FUNCTION MANIPULATORJanuary 3, 1992
K914585GRIESHABER TWO FUNCTION MANIPULATORJanuary 3, 1992
K897119GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEPApril 12, 1990
K900714ZZIPP INSTANT BOVIE CLEANERMarch 27, 1990
K890782GRIESHABER SOFT TIP NEEDLE (20 & 19 GAUGES)June 23, 1989
K890783GRIESHABER VISCOELASTIC INJECTION SYSTEMMay 16, 1989
K884043GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGENovember 16, 1988
K863444GRIESHABER GLOBAL CONTROL TUBING SETOctober 31, 1986
K864056GRIESHABER AIR SYSTEM/PRESSURE OPHTHALMIC IRRIGANTOctober 31, 1986
K860479GREEN-LINE BIPOLAR COAGULATION UNITMay 1, 1986
K860502G.A.S./GRIESHABER AIR SYSTEMFebruary 27, 1986