PROFILE SERIES 29 FILES— 510(k) K933582

Substantially Equivalent

Tulsa Dental Products, Ltd.

FDA 510(k) clearance K933582 for PROFILE SERIES 29 FILES, Substantially Equivalent on 1993-10-20. Applicant: Tulsa Dental Products, Ltd..

Clearance details

Applicant: Tulsa Dental Products, Ltd.
Product code: Code EKS
Advisory panel: Dental
Date received: 1993-07-23
Decision date: 1993-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tulsa, OK, US

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Adverse events under product code EKS

product code EKS

Malfunction: 1,949
Total: 1,949

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.