FDA 510(k) Applications Submitted by BIOMONDE

FDA 510(k) Number Submission Date Device Name Applicant
K131221 04/30/2013 LARVAL DEBRIDEMENT THERAPY PRODUCTS - BIOBAG 50/100/200/300/400 BIOMONDE
K142020 07/25/2014 LARVAL DEBRIDEMENT THERAPY PRODUCTS - LARVAE 100/200/300 AND BIOBAG 50/100/200/300/400 BIOMONDE


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