FDA 510(k) Applications Submitted by JOHN A STEEN

FDA 510(k) Number Submission Date Device Name Applicant
K020292 01/28/2002 UTERINE INJECTOR CATHETER RESEARCH, INC.
K092579 08/17/2009 INTRAUTERINE INSEMINATION (IUI) CATHETER FERTILIGENT, LTD
K032835 09/11/2003 H/S CATHETER SET CATHETER RESEARCH, INC.
K973839 10/08/1997 DISPOSABLE ESOPHAGEAL STETHOSCOPE CATHETER RESEARCH, INC.
K974357 11/19/1997 UTERINE MANIPULATOR/INJECTOR CATHETER RESEARCH, INC.


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