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FDA 510(k)

LUMINOS Q.namix T; LUMINOS Q.namix R

K-Number: K250660 · 2025-07-14

ApplicantSiemens Medical Solutions
Decision Date2025-07-14
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LUMINOS Q.namix T; LUMINOS Q.namix R is a medical device manufactured by Siemens Medical Solutions. It received FDA 510(k) clearance on 2025-07-14 under approval number K250660. 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 LUMINOS Q.namix T; LUMINOS Q.namix R?

LUMINOS Q.namix T; LUMINOS Q.namix R is a medical device that received FDA 510(k) clearance on 2025-07-14. It is manufactured by Siemens Medical Solutions. The 510(k) number is K250660.

When was LUMINOS Q.namix T; LUMINOS Q.namix R approved by the FDA?

LUMINOS Q.namix T; LUMINOS Q.namix R received FDA 510(k) clearance on 2025-07-14, under approval number K250660.

What company makes LUMINOS Q.namix T; LUMINOS Q.namix R?

LUMINOS Q.namix T; LUMINOS Q.namix R is manufactured by Siemens Medical Solutions.

What is the FDA product code for LUMINOS Q.namix T; LUMINOS Q.namix R?

The FDA product code for LUMINOS Q.namix T; LUMINOS Q.namix R 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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