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FDA 510(k)

DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2

K-Number: K072985 · 2008-06-20

ApplicantDuckworth & Kent, Ltd.
Decision Date2008-06-20
Product CodeKYB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2 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 2008-06-20 under 510(k) number K072985. The device is classified under product code KYB. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2?

DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2 is a medical device that received FDA 510(k) clearance on 2008-06-20. The listed applicant is Duckworth & Kent, Ltd.. The 510(k) number is K072985.

When did DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2 receive FDA 510(k) clearance?

DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2 received FDA 510(k) clearance on 2008-06-20, under 510(k) number K072985.

Who is the listed applicant for DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2?

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 INJECTOR, MODEL: DK7797-2?

The FDA product code for DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2 is KYB.

Related Clinical Trials

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.

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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 DK7786K060995DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM, MODEL DK7788K053176DUCKWORTH & KENT LTD CARTRIDGE LENS DELIVERY SYSTEM, MODEL DK7797K042478CAPSULE TENSION RING INSERTER, MODEL 7-810K024072DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM

Related Devices (Code: KYB)

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 DK7786Duckworth & Kent, Ltd.K070669IOL INJECTOR SETMedicel AGK063155MONARCH III IOL DELIVERY SYSTEMAlcon Manufacturing, Ltd.K063694AKREOS SINGLE USE INSERTION DEVICE, MODEL AI-28Bausch & Lomb, Inc.K032412RE-USEABLE MICROSTAAR INJECTOR, MSI-SStaar Surgical Co.K022723MASTEL 1 FOLDER IMPLANTATION SYSTEMMastel Precision, 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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