ACCUTORQ II— 510(k) K760929

Substantially Equivalent

Ritter Co.

FDA 510(k) clearance K760929 for ACCUTORQ II, Substantially Equivalent on 1976-11-19. Applicant: Ritter Co..

Clearance details

Applicant: Ritter Co.
Product code: Code EFB
Advisory panel: Dental
Date received: 1976-10-29
Decision date: 1976-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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.