INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE— 510(k) K890300

Substantially Equivalent

CooperVision, Inc.

FDA 510(k) clearance K890300 for INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE, Substantially Equivalent on 1989-04-17. Applicant: CooperVision, Inc..

Clearance details

Applicant: CooperVision, Inc.
Product code: Code HQE
Advisory panel: Ophthalmic
Date received: 1989-01-19
Decision date: 1989-04-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

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Adverse events under product code HQE

product code HQE

Injury: 156
Malfunction: 565
Total: 721

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.