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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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