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FDA 510(k) Applications Submitted by KEITH SAMOLYK
FDA 510(k) Number
Submission Date
Device Name
Applicant
K031150
04/10/2003
HEMOBAG, MODEL HBBSD2000
GLOBAL BLOOD RESOURCES, LLC
K031151
04/10/2003
TS3 TUBING SET
GLOBAL BLOOD RESOURCES, LLC
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