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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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