DUCKWORTH & KENT LTD CARTRIDGE LENS DELIVERY SYSTEM, MODEL DK7797— 510(k) K053176

Substantially Equivalent

Duckworth & Kent, Ltd.

FDA 510(k) clearance K053176 for DUCKWORTH & KENT LTD CARTRIDGE LENS DELIVERY SYSTEM, MODEL DK7797, Substantially Equivalent on 2006-01-30. Applicant: Duckworth & Kent, Ltd..

Clearance details

Applicant: Duckworth & Kent, Ltd.
Product code: Code MSS
Advisory panel: Ophthalmic
Date received: 2005-11-14
Decision date: 2006-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Baldock, Hertfordshire, GB

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Adverse events under product code MSS

product code MSS

Injury: 385
Malfunction: 2,033
Total: 2,418

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.