HIGH FUSING YELLOW CERAMIC SOLDER
K-Number: K895059 · 1990-10-05
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Device Summary
Frequently Asked Questions
What is the HIGH FUSING YELLOW CERAMIC SOLDER?
HIGH FUSING YELLOW CERAMIC SOLDER is a medical device that received FDA 510(k) clearance on 1990-10-05. The listed applicant is Leach and Dillon Co., Inc.. The 510(k) number is K895059.
When did HIGH FUSING YELLOW CERAMIC SOLDER receive FDA 510(k) clearance?
HIGH FUSING YELLOW CERAMIC SOLDER received FDA 510(k) clearance on 1990-10-05, under 510(k) number K895059.
Who is the listed applicant for HIGH FUSING YELLOW CERAMIC SOLDER?
The FDA 510(k) record lists Leach and Dillon Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HIGH FUSING YELLOW CERAMIC SOLDER?
The FDA product code for HIGH FUSING YELLOW CERAMIC SOLDER 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 Leach and Dillon Co., 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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