ALARIS SYSTEM WITH MMS, MODEL 8XXX (K072105) — FDA 510(k) Clearance | Predicase

K-number	K072105
Device name	ALARIS SYSTEM WITH MMS, MODEL 8XXX
Applicant	Cardinal Health 303,Inc.
Product code	FRN
Device class	Class II
Decision date	Dec 28, 2007
Decision	Substantially Equivalent
Regulation	880.5725

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Source

View the full FDA submission: accessdata.fda.gov

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