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FDA 510(k)

QUICKCAT EXTRACTION CATHETER, MODEL 60090-01

K-Number: K073519 · 2008-03-28

ApplicantKensey Nash Corp.
Decision Date2008-03-28
Product CodeQEZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

QUICKCAT EXTRACTION CATHETER, MODEL 60090-01 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 2008-03-28 under 510(k) number K073519. 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, MODEL 60090-01?

QUICKCAT EXTRACTION CATHETER, MODEL 60090-01 is a medical device that received FDA 510(k) clearance on 2008-03-28. The listed applicant is Kensey Nash Corp.. The 510(k) number is K073519.

When did QUICKCAT EXTRACTION CATHETER, MODEL 60090-01 receive FDA 510(k) clearance?

QUICKCAT EXTRACTION CATHETER, MODEL 60090-01 received FDA 510(k) clearance on 2008-03-28, under 510(k) number K073519.

Who is the listed applicant for QUICKCAT EXTRACTION CATHETER, MODEL 60090-01?

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, MODEL 60090-01?

The FDA product code for QUICKCAT EXTRACTION CATHETER, MODEL 60090-01 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 MEMBRANEK071695KENSEY NASH MACROPORE SHIELDK072384MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & PASTE

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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.

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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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