TEK-LUBE
K-Number: K925080 · 1994-01-31
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Device Summary
Frequently Asked Questions
What is the TEK-LUBE?
TEK-LUBE is a medical device that received FDA 510(k) clearance on 1994-01-31. The listed applicant is Clinical Technology Corp.. The 510(k) number is K925080.
When did TEK-LUBE receive FDA 510(k) clearance?
TEK-LUBE received FDA 510(k) clearance on 1994-01-31, under 510(k) number K925080.
Who is the listed applicant for TEK-LUBE?
The FDA 510(k) record lists Clinical Technology Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TEK-LUBE?
The FDA product code for TEK-LUBE is EFB.
Other records listing Clinical Technology 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: EFB)
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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