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Omnitech Systems, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K151976Omnitech HF Resection Electrodes, Omnitech HF Vaporization ElectrodeJune 27, 2016
K050454OMNITECH FULGURATING ELECTRODEMay 27, 2005
K981463OMNITECH RESECTOSCOPE ROLLER ELECTRODEJuly 17, 1998
K981464OMNITECH RESECTOSCOPE CUTTING LOOP ELECTRODEJuly 10, 1998
K964365RESECTOSCOPE CUTTING LOOP ELECTRODEApril 22, 1997
K965093OMNITECH RESECTOSCOPE ROLLER ELECTRODEMarch 19, 1997