AOI UNIVERSAL ULTRASONIC HANDPIECE— 510(k) K950880

Substantially Equivalent

American Optical Corp.

FDA 510(k) clearance K950880 for AOI UNIVERSAL ULTRASONIC HANDPIECE, Substantially Equivalent on 1995-05-26. Applicant: American Optical Corp..

Clearance details

Applicant: American Optical Corp.
Product code: Code HQC
Advisory panel: Ophthalmic
Date received: 1995-02-27
Decision date: 1995-05-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

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Adverse events under product code HQC

product code HQC

Injury: 2,378
Malfunction: 8,768
Total: 11,146

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.