FDA 510(k) Applications Submitted by STIHLER ELECTRONIC GMBH

FDA 510(k) Number Submission Date Device Name Applicant
K202197 08/05/2020 Astopad Patient Warming System Stihler Electronic GmbH
K020103 01/11/2002 PRISMAFLO STIHLER ELECTRONIC GMBH
K991159 04/07/1999 PRISMATHERM II, ASTOLINE STIHLER ELECTRONIC GMBH
K991160 04/07/1999 ASTOTHERM PLUS, ASTOTUBES, ASTOLINE STIHLER ELECTRONIC GMBH
K082758 09/19/2008 PRISMAFLO II STIHLER ELECTRONIC GMBH
K082765 09/22/2008 ASTOFLO PLUS STIHLER ELECTRONIC GMBH


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