FDA 510(k) Applications Submitted by DATEX-OHMEDA INC., A DIVISION OF INSTRUMENTARIUM C

FDA 510(k) Number Submission Date Device Name Applicant
K092864 09/17/2009 AESPIRE 7900, AESPIRE VIEW DATEX-OHMEDA INC., A DIVISION OF INSTRUMENTARIUM C
K093886 12/18/2009 ENGSTROM CARESTATION, ENGSTROM PRO DATEX-OHMEDA INC., A DIVISION OF INSTRUMENTARIUM C


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