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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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