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FDA 510(k)

ARTERIAL HEALTH PACKAGE (AHP) SOFTWARE

K-Number: K083149 · 2009-01-14

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2009-01-14
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARTERIAL HEALTH PACKAGE (AHP) SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2009-01-14 under 510(k) number K083149. 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 ARTERIAL HEALTH PACKAGE (AHP) SOFTWARE?

ARTERIAL HEALTH PACKAGE (AHP) SOFTWARE is a medical device that received FDA 510(k) clearance on 2009-01-14. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K083149.

When did ARTERIAL HEALTH PACKAGE (AHP) SOFTWARE receive FDA 510(k) clearance?

ARTERIAL HEALTH PACKAGE (AHP) SOFTWARE received FDA 510(k) clearance on 2009-01-14, under 510(k) number K083149.

Who is the listed applicant for ARTERIAL HEALTH PACKAGE (AHP) SOFTWARE?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTERIAL HEALTH PACKAGE (AHP) SOFTWARE?

The FDA product code for ARTERIAL HEALTH PACKAGE (AHP) SOFTWARE is LLZ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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