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FDA 510(k)

MCKESSON HORIZON CARDIOLOGY

K-Number: K112720 · 2012-01-30

ApplicantMckesson Israel , Ltd.
Decision Date2012-01-30
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MCKESSON HORIZON CARDIOLOGY is the device name listed in this FDA 510(k) record. The listed applicant is Mckesson Israel , Ltd.. It received FDA 510(k) clearance on 2012-01-30 under 510(k) number K112720. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MCKESSON HORIZON CARDIOLOGY?

MCKESSON HORIZON CARDIOLOGY is a medical device that received FDA 510(k) clearance on 2012-01-30. The listed applicant is Mckesson Israel , Ltd.. The 510(k) number is K112720.

When did MCKESSON HORIZON CARDIOLOGY receive FDA 510(k) clearance?

MCKESSON HORIZON CARDIOLOGY received FDA 510(k) clearance on 2012-01-30, under 510(k) number K112720.

Who is the listed applicant for MCKESSON HORIZON CARDIOLOGY?

The FDA 510(k) record lists Mckesson Israel , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MCKESSON HORIZON CARDIOLOGY?

The FDA product code for MCKESSON HORIZON CARDIOLOGY is LLZ.

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Other records listing Mckesson Israel , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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