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FDA 510(k)

DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM

K-Number: K024072 · 2003-10-06

ApplicantDuckworth & Kent, Ltd.
Decision Date2003-10-06
Product CodeMSS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Duckworth & Kent, Ltd.. It received FDA 510(k) clearance on 2003-10-06 under 510(k) number K024072. The device is classified under product code MSS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM?

DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 2003-10-06. The listed applicant is Duckworth & Kent, Ltd.. The 510(k) number is K024072.

When did DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM receive FDA 510(k) clearance?

DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM received FDA 510(k) clearance on 2003-10-06, under 510(k) number K024072.

Who is the listed applicant for DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM?

The FDA 510(k) record lists Duckworth & Kent, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM?

The FDA product code for DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM is MSS.

Related Clinical Trials

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Other records listing Duckworth & Kent, Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K081382DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786K072985DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2K060995DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM, MODEL DK7788K053176DUCKWORTH & KENT LTD CARTRIDGE LENS DELIVERY SYSTEM, MODEL DK7797K042478CAPSULE TENSION RING INSERTER, MODEL 7-810

Related Devices (Code: MSS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261174RxSight® Insertion DeviceRxsight, Inc.K252540ACCUJECT Injector Set 2.1-1P (LP604590)Medicel AGK242389EyeGility™ Inserter for Preloaded enVista IOLsBausch & Lomb, IncorporatedK231106Accuject Refra Injector AR2900Medicel AGK231838RxSight® Insertion Device (63002)Rxsight, Inc.K231466RxSight Insertion DeviceRxsight, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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