CLAYTON INTRA-AURAL DEVICE (CID)— 510(k) K091880

Substantially Equivalent

Ascentia Health Incorporated

FDA 510(k) clearance K091880 for CLAYTON INTRA-AURAL DEVICE (CID), Substantially Equivalent on 2010-02-24. Applicant: Ascentia Health Incorporated.

Clearance details

Applicant: Ascentia Health Incorporated
Product code: Code MQC
Advisory panel: Unknown
Date received: 2009-06-24
Decision date: 2010-02-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Springfield, VA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MQC

product code MQC

Injury: 377
Total: 377

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.