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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