THE WESTERN CORTICAL ELECTRODE ARRAY
K-Number: K923330 · 1993-11-09
Advertisement
Device Summary
Frequently Asked Questions
What is the THE WESTERN CORTICAL ELECTRODE ARRAY?
THE WESTERN CORTICAL ELECTRODE ARRAY is a medical device that received FDA 510(k) clearance on 1993-11-09. The listed applicant is University Hospital (London) Development Corp.. The 510(k) number is K923330.
When did THE WESTERN CORTICAL ELECTRODE ARRAY receive FDA 510(k) clearance?
THE WESTERN CORTICAL ELECTRODE ARRAY received FDA 510(k) clearance on 1993-11-09, under 510(k) number K923330.
Who is the listed applicant for THE WESTERN CORTICAL ELECTRODE ARRAY?
The FDA 510(k) record lists University Hospital (London) Development Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THE WESTERN CORTICAL ELECTRODE ARRAY?
The FDA product code for THE WESTERN CORTICAL ELECTRODE ARRAY is GYC.
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.
Related Devices (Code: GYC)
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.
Advertisement