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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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