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FDA 510(k)

KENSEY NASH WUIK-SERT(TM) ENDOSCOPIC SURG GRASPER

K-Number: K926089 · 1993-07-23

ApplicantKensey Nash Corp.
Decision Date1993-07-23
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KENSEY NASH WUIK-SERT(TM) ENDOSCOPIC SURG GRASPER 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 1993-07-23 under 510(k) number K926089. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KENSEY NASH WUIK-SERT(TM) ENDOSCOPIC SURG GRASPER?

KENSEY NASH WUIK-SERT(TM) ENDOSCOPIC SURG GRASPER is a medical device that received FDA 510(k) clearance on 1993-07-23. The listed applicant is Kensey Nash Corp.. The 510(k) number is K926089.

When did KENSEY NASH WUIK-SERT(TM) ENDOSCOPIC SURG GRASPER receive FDA 510(k) clearance?

KENSEY NASH WUIK-SERT(TM) ENDOSCOPIC SURG GRASPER received FDA 510(k) clearance on 1993-07-23, under 510(k) number K926089.

Who is the listed applicant for KENSEY NASH WUIK-SERT(TM) ENDOSCOPIC SURG GRASPER?

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 KENSEY NASH WUIK-SERT(TM) ENDOSCOPIC SURG GRASPER?

The FDA product code for KENSEY NASH WUIK-SERT(TM) ENDOSCOPIC SURG GRASPER is GCJ.

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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: GCJ)

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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