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FDA 510(k)

AXIOM LUMINOS DRF

K-Number: K062623 · 2007-08-22

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2007-08-22
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AXIOM LUMINOS DRF 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 2007-08-22 under 510(k) number K062623. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AXIOM LUMINOS DRF?

AXIOM LUMINOS DRF is a medical device that received FDA 510(k) clearance on 2007-08-22. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K062623.

When did AXIOM LUMINOS DRF receive FDA 510(k) clearance?

AXIOM LUMINOS DRF received FDA 510(k) clearance on 2007-08-22, under 510(k) number K062623.

Who is the listed applicant for AXIOM LUMINOS DRF?

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 LUMINOS DRF?

The FDA product code for AXIOM LUMINOS DRF is OWB.

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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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