TEK-LUBE— 510(k) K925080

Substantially Equivalent

Clinical Technology Corp.

FDA 510(k) clearance K925080 for TEK-LUBE, Substantially Equivalent on 1994-01-31. Applicant: Clinical Technology Corp..

Clearance details

Applicant: Clinical Technology Corp.
Product code: Code EFB
Advisory panel: Dental
Date received: 1992-10-07
Decision date: 1994-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Scottsdale, AZ, US

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Adverse events under product code EFB

product code EFB

Injury: 133
Malfunction: 562
Total: 695

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.