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FDA 510(k)

QUICKCAT EXTRACTION CATHETER

K-Number: K060092 · 2006-03-09

ApplicantKensey Nash Corp.
Decision Date2006-03-09
Product CodeQEZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

QUICKCAT EXTRACTION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Kensey Nash Corp.. It received FDA 510(k) clearance on 2006-03-09 under 510(k) number K060092. The device is classified under product code QEZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICKCAT EXTRACTION CATHETER?

QUICKCAT EXTRACTION CATHETER is a medical device that received FDA 510(k) clearance on 2006-03-09. The listed applicant is Kensey Nash Corp.. The 510(k) number is K060092.

When did QUICKCAT EXTRACTION CATHETER receive FDA 510(k) clearance?

QUICKCAT EXTRACTION CATHETER received FDA 510(k) clearance on 2006-03-09, under 510(k) number K060092.

Who is the listed applicant for QUICKCAT EXTRACTION CATHETER?

The FDA 510(k) record lists Kensey Nash Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUICKCAT EXTRACTION CATHETER?

The FDA product code for QUICKCAT EXTRACTION CATHETER is QEZ.

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Other records listing Kensey Nash Corp. 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.

K103787MEDEOR MATRIXK091192KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XXK091499MEDEOR MATRIX, MODELS 30010-XX (HYDRATED); 30020-XX (DRY)K090919KENSEY NASH FIBRILLAR COLLAGEN DENTAL MEMBRANEK073519QUICKCAT EXTRACTION CATHETER, MODEL 60090-01K071695KENSEY NASH MACROPORE SHIELD

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Related Devices (Code: QEZ)

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.

K254035Mayumi™ Thrombectomy SystemMicroVention, Inc., d/b/a Terumo NeuroK261105Powered Aventus Thrombectomy System™Inquis MedicalK262030Aventus Thrombectomy SystemInquis MedicalK253589Liberant™ RX Aspiration CatheterMedtronic Interventional Vascular, Inc.K254208FLOWRUNNER Aspiration SystemExpanse Medical, Inc.K253925Aventus Thrombectomy SystemInquis Medical

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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