FDA 510(k) Applications Submitted by WAYNE STERNER

FDA 510(k) Number Submission Date Device Name Applicant
K012758 08/17/2001 URETEROSCOPE, PEDIATRIC CYSTOURETEROSCOPE, OPERATING PEDIATRIC CYSTOURETEROSCOPE, MODELS MR-9, MR-9L, CIRCON VIDEO
K012925 08/31/2001 DUR-8, MODELS DUR-8 CIRCON VIDEO
K012929 08/31/2001 FLEXIBLE PEDIATRIC CYSTOURETEROSCOPE, MODEL AUR- 735 CIRCON VIDEO
K000669 02/28/2000 MEDIVISION I-VIEW PERSONAL VIDEO DISPLAY MEDIVISION ENDOSCOPY
K971995 05/30/1997 MEDIVISION SINOSCOPE MEDIVISION SCOPE SERVICE CENTER, INC.
K971996 05/30/1997 MEDIVISION ARTHROSCOP MEDIVISION SCOPE SERVICE CENTER, INC.
K011849 06/13/2001 MICRO-6-SERIES (MR-6, MR-6L) URETEROSCOPES, MRO-6 SERIES (MR-633, MR-642) URETEROSCOPES, MRO-7 SERIES (MRO-733) URETEROS CIRCON VIDEO
K012265 07/19/2001 METAL HALIDE LIGHT SOURCE, MODELS MV-9088-T, MV-9088 CIRCON VIDEO
K982620 07/27/1998 MEDIVISION CYSTOSCOPE MEDIVISION SCOPE SERVICE CENTER, INC.
K982659 07/30/1998 MEDIVISION HYSTEROSCOPE MEDIVISION SCOPE SERVICE CENTER, INC.
K012951 09/04/2001 APN-2 USA SERIES FLEXIBLE CHOLEDOCHOSCOPE CIRCON VIDEO
K013165 09/21/2001 USA SERIES LAPAROSCOPES CIRCON ACMI
K984434 12/14/1998 MEDIVISION LAPAROSCOPE MEDIVISION SCOPE SERVICE CENTER, INC.


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