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FDA 510(k)

ALARIS SYSTEM WITH MMS, MODEL 8XXX

K-Number: K072105 · 2007-12-28

ApplicantCardinal Health 303,Inc.
Decision Date2007-12-28
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALARIS SYSTEM WITH MMS, MODEL 8XXX is the device name listed in this FDA 510(k) record. The listed applicant is Cardinal Health 303,Inc.. It received FDA 510(k) clearance on 2007-12-28 under 510(k) number K072105. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALARIS SYSTEM WITH MMS, MODEL 8XXX?

ALARIS SYSTEM WITH MMS, MODEL 8XXX is a medical device that received FDA 510(k) clearance on 2007-12-28. The listed applicant is Cardinal Health 303,Inc.. The 510(k) number is K072105.

When did ALARIS SYSTEM WITH MMS, MODEL 8XXX receive FDA 510(k) clearance?

ALARIS SYSTEM WITH MMS, MODEL 8XXX received FDA 510(k) clearance on 2007-12-28, under 510(k) number K072105.

Who is the listed applicant for ALARIS SYSTEM WITH MMS, MODEL 8XXX?

The FDA 510(k) record lists Cardinal Health 303,Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALARIS SYSTEM WITH MMS, MODEL 8XXX?

The FDA product code for ALARIS SYSTEM WITH MMS, MODEL 8XXX is FRN.

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Official Source

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