FDA 510(k) Applications Submitted by DENIS DORSEY

FDA 510(k) Number Submission Date Device Name Applicant
K020628 02/26/2002 CURELLE, PREFERRED CURELLE, CUTEQ 2.5 BIOTEQUE AMERICA, INC.
K041094 04/27/2004 HSG CATHETER SET BIOTEQUE AMERICA, INC.
K013289 10/02/2001 BIOTEQUE VAGINAL PESSARIES BIOTEQUE AMERICA, INC.
K003380 10/31/2000 BIOTEQUE VAGINAL DILATOR BIOTEQUE AMERICA, INC.


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