FDA 510(k) Applications Submitted by Ulrike Zeissler

FDA 510(k) Number Submission Date Device Name Applicant
K171869 06/22/2017 Sutter CURIS RF Generator Sutter Medizintechnik GmbH
K191732 06/28/2019 Sutter RaVoR Bipolar Electrodes Sutter Medizintechnik GmbH
K192128 08/07/2019 Sutter Arrowtip Monopolar Electrodes Sutter Medizintechnik GmbH
K193587 12/23/2019 Sutter Swyng non-stick bipolar forceps, single-use Sutter Medizintechnik GmbH


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