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FDA 510(k) Applications Submitted by RENE RONCKEN
FDA 510(k) Number
Submission Date
Device Name
Applicant
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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