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FDA 510(k)

TEK-LUBE

K-Number: K925080 · 1994-01-31

Decision Date1994-01-31
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TEK-LUBE is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Technology Corp.. It received FDA 510(k) clearance on 1994-01-31 under 510(k) number K925080. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 12 devices →

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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