FDA 510(k) Applications Submitted by Claudia Winterschladen

FDA 510(k) Number Submission Date Device Name Applicant
K223542 11/25/2022 TubaVent Balloon Dilatation System Spiggle & Theis Medizintechnik GmbH
K123699 12/03/2012 FAHL TRACHEOSTOMY TUBES (MULTIPLE) ANDREAS FAHL MEDIZINTECHNIK-VERTRIEB GMBH


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