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


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact