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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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