ELOQUENCE, INTEGRATED FUNCTIONAL IMAGING SYSTEM
K-Number: K023130 · 2002-10-11
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Device Summary
Frequently Asked Questions
What is the ELOQUENCE, INTEGRATED FUNCTIONAL IMAGING SYSTEM?
ELOQUENCE, INTEGRATED FUNCTIONAL IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 2002-10-11. The listed applicant is Mri Devices Corp.. The 510(k) number is K023130.
When did ELOQUENCE, INTEGRATED FUNCTIONAL IMAGING SYSTEM receive FDA 510(k) clearance?
ELOQUENCE, INTEGRATED FUNCTIONAL IMAGING SYSTEM received FDA 510(k) clearance on 2002-10-11, under 510(k) number K023130.
Who is the listed applicant for ELOQUENCE, INTEGRATED FUNCTIONAL IMAGING SYSTEM?
The FDA 510(k) record lists Mri Devices Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELOQUENCE, INTEGRATED FUNCTIONAL IMAGING SYSTEM?
The FDA product code for ELOQUENCE, INTEGRATED FUNCTIONAL IMAGING SYSTEM is LNH.
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 Mri Devices Corp. 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.
Related Devices (Code: LNH)
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.
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