INNOVA TELESCOPIC DISTRACTOR— 510(k) K984117

Substantially Equivalent

Innova Corp.

FDA 510(k) clearance K984117 for INNOVA TELESCOPIC DISTRACTOR, Substantially Equivalent on 1999-02-10. Applicant: Innova Corp..

Clearance details

Applicant: Innova Corp.
Product code: Code MQN
Advisory panel: Dental
Date received: 1998-11-17
Decision date: 1999-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MQN

product code MQN

Injury: 346
Total: 346

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.