PHACOEMULSIFICATION UNIT TO REMOVE CATARAC. LENS— 510(k) K894512

Substantially Equivalent

Intl. Ophthalmic Industries Corp.

FDA 510(k) clearance K894512 for PHACOEMULSIFICATION UNIT TO REMOVE CATARAC. LENS, Substantially Equivalent on 1989-10-17. Applicant: Intl. Ophthalmic Industries Corp..

Clearance details

Applicant: Intl. Ophthalmic Industries Corp.
Product code: Code HQC
Advisory panel: Ophthalmic
Date received: 1989-07-19
Decision date: 1989-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Weston, MA, 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.