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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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