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FDA 510(k) Applications Submitted by EILEEN DORSEY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130520
02/28/2013
CAPIOX FX15 AND FX25 HOLLOW FIBER OXYGENATOR/RESERVOIR
ASHITAKA FACTORY OF TERUMO CORP.
K140774
03/28/2014
TERUMO CAPIOX FX15 AND FX25 HOLLOW FIBER OXYGENATOR/RESERVOIR
Terumo Cardiovascular Systems Corporation
K071630
06/14/2007
TERUMO 31G THINPRO INSULIN SYRINGE
TERUMO MEDICAL CORP.
K221895
06/30/2022
Terumo Advanced Perfusion System 1
Terumo Cardiovascular Systems Corporation
K082362
08/18/2008
SURSHIELD SAFETY I.V. CATHETER
TERUMO MEDICAL CORP.
K082997
10/08/2008
TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER
TERUMO MEDICAL CORP.
K083834
12/23/2008
TERUMO PALL AL6X ARTERIAL FILTER
TERUMO CARDIOVASCULAR SYSTEMS CORP.
K093992
12/24/2009
TERUMO LAUER LOCK ADAPTER
Terumo Cardiovascular Systems Corporation
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