DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2— 510(k) K072985

Name: FDA 510(k) clearance K072985
Creator: U.S. Food and Drug Administration
Published: 2008-06-20

Substantially Equivalent

Duckworth & Kent, Ltd.

FDA 510(k) clearance K072985 for DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2, Substantially Equivalent on 2008-06-20. Applicant: Duckworth & Kent, Ltd.. Device class: 1.

Clearance details

Applicant: Duckworth & Kent, Ltd.
Product code: Code KYB
Device class: Class 1
Regulation: 21 CFR 886.4300
Advisory panel: Ophthalmic
Date received: 2007-10-23
Decision date: 2008-06-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Baldock, Hertfordshire, GB

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KYB

product code KYB

Injury: 218
Malfunction: 1,989
Other: 1
Total: 2,208

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.