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Bergen Mfg.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K972299BERGEN MODEL 500 ELECTROSURGERY GENERATORAugust 27, 1997
K964736BERGEN 610 BIPOLAR COAGULATORFebruary 27, 1997
K945861BERGEN 710 ESUMarch 1, 1995
K863701MODEL 709 BIPOLAR MICRO COAGULATOROctober 14, 1986