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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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