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FDA 510(k) Applications Submitted by BERGEN MFG.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K972299
06/19/1997
BERGEN MODEL 500 ELECTROSURGERY GENERATOR
BERGEN MFG.
K964736
11/25/1996
BERGEN 610 BIPOLAR COAGULATOR
BERGEN MFG.
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