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FDA 510(k)

AXIOM ARISTOS FX PLUS

K-Number: K061054 · 2006-05-09

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2006-05-09
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AXIOM ARISTOS FX PLUS 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 2006-05-09 under 510(k) number K061054. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AXIOM ARISTOS FX PLUS?

AXIOM ARISTOS FX PLUS is a medical device that received FDA 510(k) clearance on 2006-05-09. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K061054.

When did AXIOM ARISTOS FX PLUS receive FDA 510(k) clearance?

AXIOM ARISTOS FX PLUS received FDA 510(k) clearance on 2006-05-09, under 510(k) number K061054.

Who is the listed applicant for AXIOM ARISTOS FX PLUS?

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 AXIOM ARISTOS FX PLUS?

The FDA product code for AXIOM ARISTOS FX PLUS is MQB.

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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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