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FDA 510(k) Applications Submitted by BIOTEQUE AMERICA, INC.
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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