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FDA 510(k) Applications Submitted by BIOCORE MEDICAL TECHNOLOGIES, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K012990
09/06/2001
COLLATEK POWDER
BIOCORE MEDICAL TECHNOLOGIES, INC.
K012995
09/06/2001
COLLATEK SHEET
BIOCORE MEDICAL TECHNOLOGIES, INC.
K012997
09/06/2001
COLLATEK FOAM
BIOCORE MEDICAL TECHNOLOGIES, INC.
K022995
09/09/2002
COLLATEK HYDROGEL
BIOCORE MEDICAL TECHNOLOGIES, INC.
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