FDA 510(k) Applications Submitted by BRANDI JAMES

FDA 510(k) Number Submission Date Device Name Applicant
K100543 02/25/2010 MEDISSISS REPROCESSEDENT ABLATION WANDS (COBLATORS), MODEL#EIC8872-01 MEDISISS
K081559 06/03/2008 GENESIS MEDISISS
K042659 09/28/2004 MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS MEDISISS


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