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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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