FDA 510(k) Applications for Medical Device Product Code "FDC"
(Resectoscope, Working Element)

FDA 510(k) Number Applicant Device Name Decision Date
K021166 ACMI-CIRCON CORPORATION ACMI BIPOLAR RECTOSCOPE, MODEL EIWE-BR 05/09/2002
K991426 MAHE INTL., INC. MAHE INSTRUMENTS 08/05/1999
K992141 OLYMPUS WINTER & IBE GMBH OLYMPUS WORKING ELEMENT FOR PROBES 09/29/1999


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