Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ONCOR EXPRESSION

K-Number: K060226 · 2006-03-15

Decision Date2006-03-15
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ONCOR EXPRESSION 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 2006-03-15 under 510(k) number K060226. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ONCOR EXPRESSION?

ONCOR EXPRESSION is a medical device that received FDA 510(k) clearance on 2006-03-15. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K060226.

When did ONCOR EXPRESSION receive FDA 510(k) clearance?

ONCOR EXPRESSION received FDA 510(k) clearance on 2006-03-15, under 510(k) number K060226.

Who is the listed applicant for ONCOR EXPRESSION?

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 ONCOR EXPRESSION?

The FDA product code for ONCOR EXPRESSION is IYE.

Related Clinical Trials

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.

Other records listing Siemens Medical Solutions USA, Inc. 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.

View all 732 devices →

Related Devices (Code: IYE)

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.

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.

↑