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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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