FDA 510(k) Applications Submitted by LOUISE MUSANTE

FDA 510(k) Number Submission Date Device Name Applicant
K090752 03/20/2009 PENUMBRA SYSTEM (PENNUMBRA REPERFUSION CATHETER 054), MODEL PSC054; (PENUMBRA SEPARATOR 054), MODEL PSS054 PENUMBRA, INC.
K200904 04/06/2020 Tosoh Automated Glycohemoglobin Analyzer HLC-723G8 Tosoh Bioscience, Inc.
K131026 04/12/2013 BOSCH BLOOD PRESSURE METER (BP5000 BT) ROBERT BOSCH HEALTHCARE SYSTEMS, INC.
K211199 04/22/2021 ST AIA-PACK BNP Assay Tosoh Bioscience, Inc.


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