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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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