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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact