Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786

K-Number: K081382 · 2008-10-23

ApplicantDuckworth & Kent, Ltd.
Decision Date2008-10-23
Product CodeKYB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786 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 2008-10-23 under 510(k) number K081382. 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., IMPLANTATION SYSTEM, MODEL DK7786?

DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786 is a medical device that received FDA 510(k) clearance on 2008-10-23. The listed applicant is Duckworth & Kent, Ltd.. The 510(k) number is K081382.

When did DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786 receive FDA 510(k) clearance?

DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786 received FDA 510(k) clearance on 2008-10-23, under 510(k) number K081382.

Who is the listed applicant for DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786?

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., IMPLANTATION SYSTEM, MODEL DK7786?

The FDA product code for DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K072985DUCKWORTH & 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 7-810K024072DUCKWORTH & 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.

K072985DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2Duckworth & 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.

↑