FIBRA-SONICS PHACO III OR IIIP FRAGMENTATION SYSTEM— 510(k) K984143

Substantially Equivalent

Fibra Sonics, Inc.

FDA 510(k) clearance K984143 for FIBRA-SONICS PHACO III OR IIIP FRAGMENTATION SYSTEM, Substantially Equivalent on 1999-02-16. Applicant: Fibra Sonics, Inc..

Clearance details

Applicant: Fibra Sonics, Inc.
Product code: Code HQC
Advisory panel: Ophthalmic
Date received: 1998-11-18
Decision date: 1999-02-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, 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.