FDA 510(k) Applications Submitted by JOE D BROWN

FDA 510(k) Number Submission Date Device Name Applicant
K020673 03/01/2002 WAVE FORM MANUFACTURING PROLASE GENERAL SHAPED FIBER WAVE FORM MFG., INC.
K001243 04/18/2000 DORNIER MEDILAS H DORNIER SURGICAL PRODUCTS, INC.
K022338 07/18/2002 OPTICAL INTEGRITY GENERAL SHAPED FIBER OPTICAL INTEGRITY, INC.
K954904 10/25/1995 MICROQUARTZ MEDICAL GENERAL SHAPE LASER FIBER MICROQUARTZ MEDICAL, INC.


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