FDA 510(k) Applications Submitted by MEDTREX, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K970039 01/06/1997 ENCORE ELECTROSURGICAL HANDCONTROL PENCIL (35001-001) MEDTREX, INC.
K981724 05/15/1998 O.R.PRO 300 ELECTROSURGICAL GENERATOR MODEL 40001-100 MEDTREX, INC.
K970130 01/15/1997 HYDROCOOL DUAL CONDUCTOR POLYMER GEL (30101-001/CORDED DISPERSIVE ELECTRODE-SENSING MEDTREX, INC.


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