FDA 510(k) Applications Submitted by Fehling Instruments GmbH & Co. KG

FDA 510(k) Number Submission Date Device Name Applicant
K170726 03/09/2017 Biopsy Forceps Fehling Instruments GmbH & Co. KG
K153243 11/09/2015 Fehling-Punches Fehling Instruments GmbH & Co. KG


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