FDA 510(k) Applications Submitted by ELLMAN INTL., INC.

FDA 510(k) Number Submission Date Device Name Applicant
K990146 01/19/1999 SURGITRON ELLMAN INTL., INC.
K980170 01/20/1998 SURGITRON ELLMAN INTL., INC.
K980177 01/20/1998 SUGITRON MODEL: IEC ELLMAN INTL., INC.
K001253 04/19/2000 SURGITRON IEC II ELLMAN INTL., INC.
K001407 05/04/2000 SURGITRON IEC II ELLMAN INTL., INC.
K972072 06/03/1997 SURGITRON MODEL FFPF-EMC ELLMAN INTL., INC.
K001986 06/29/2000 SURGITRON IEC II ELLMAN INTL., INC.
K992382 07/16/1999 SURGITRON RADIOLASE ELLMAN INTL., INC.
K013255 09/28/2001 SURGITRON 120 IEC (ALSO KNOWN AS SURGITRON 4.0 DUAL RF ELLMAN INTL., INC.
K003126 10/05/2000 BIPOLAR TRIGGER-FLEX PROBE ELLMAN INTL., INC.
K954703 10/12/1995 MEDI-FRIG ELLMAN INTL., INC.
K954718 10/13/1995 ELLMAN NEEDLE EXTENDER/MEASURED DOSE SYRINGE ELLMAN INTL., INC.
K955158 11/13/1995 SURGITRON ELLMAN INTL., INC.
K955167 11/13/1995 SURGITRON ELLMAN INTL., INC.
K955176 11/13/1995 DENTO-SURGE ELLMAN INTL., INC.


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