FDA 510(k) Applications Submitted by BUCKMAN CONSULTANTS

FDA 510(k) Number Submission Date Device Name Applicant
K830316 01/31/1983 UNIFLEX BUCKMAN CONSULTANTS
K821829 06/22/1982 UROGARD BUCKMAN CONSULTANTS
K823882 12/27/1982 M-BRACE BUCKMAN CONSULTANTS


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