EL DORADO 40
K-Number: K964941 · 1997-01-13
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Device Summary
Frequently Asked Questions
What is the EL DORADO 40?
EL DORADO 40 is a medical device that received FDA 510(k) clearance on 1997-01-13. The listed applicant is Gateway Alloys, Inc.. The 510(k) number is K964941.
When did EL DORADO 40 receive FDA 510(k) clearance?
EL DORADO 40 received FDA 510(k) clearance on 1997-01-13, under 510(k) number K964941.
Who is the listed applicant for EL DORADO 40?
The FDA 510(k) record lists Gateway Alloys, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EL DORADO 40?
The FDA product code for EL DORADO 40 is EJT.
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 Gateway Alloys, 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.
Related Devices (Code: EJT)
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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