FDA 510(k) Applications Submitted by TECHNOMED EUROPE
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K990015 |
01/04/1999 |
ELECTRODE NEEDLES |
TECHNOMED EUROPE |
| K072016 |
07/23/2007 |
CUP ELECTRODES, GOLD, REUSABLE, SILVER, REUSABLE; CUP ELECTRODES SILVER/SILVER CHLORIDE REUSABLE |
TECHNOMED EUROPE |
| K063729 |
12/15/2006 |
DISPOSABLE PEDICLE SCREW PROBE, MODEL 3603-00 |
TECHNOMED EUROPE |
| K073532 |
12/17/2007 |
DISPOSABLE ADHESIVE SURFACE ELECTRODES, DISC ELECTRODES |
TECHNOMED EUROPE |
| K130136 |
01/18/2013 |
DISPOSABLE AND REUSABLE CONCENTRIC NEEDLE ELECTRODES,DISPOSABLE AND REUSABLE SUBDERMAL NEEDLE ELECTRODES, |
TECHNOMED EUROPE |
| K110422 |
02/14/2011 |
SURGICAL STIMULATORS |
TECHNOMED EUROPE |
| K121257 |
04/26/2012 |
LARYNGEAL ELECTRODE |
TECHNOMED EUROPE |
| K050325 |
02/09/2005 |
DISPOSABLE CONCENTRIC PROBE, DISPOSABLE BIPOLAR PROBE, DISPOSABLE MONOPOLAR PROBE |
TECHNOMED EUROPE |
| K062437 |
08/11/2006 |
DISPOSABLE HYPODERMIC EMG NEEDLE ELECTRODE TECHNOMED EUROPE VERSION AND PRIVATE LABELED |
TECHNOMED EUROPE |
| K042375 |
09/01/2004 |
SMK, CX, CXE, RCN |
TECHNOMED EUROPE |
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