FDA 510(k) Applications for Medical Device Product Code "FGM"
(Probe And Director, Gastro-Urology)

FDA 510(k) Number Applicant Device Name Decision Date
K041732 BLUE TORCH MEDICAL TECHNOLOGIES CAVERMAP SURGICAL AID 09/21/2004
K031527 BLUE TORCH MEDICAL TECHNOLOGIES MODIFICATION TO CAVERMAP SURGICAL AID 06/05/2003
K993436 UROMED CORP. CAVERMAP SURGICAL AID 02/11/2000
K010098 UROMED CORP. MODIFICATION TO CAVERMAP SURGICAL AID 02/01/2001


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