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FDA 510(k)

KENSEY NASH DYNAMIC CLIP SYSTEM

K-Number: K923726 · 1993-04-06

ApplicantKensey Nash Corp.
Decision Date1993-04-06
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KENSEY NASH DYNAMIC CLIP SYSTEM 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 1993-04-06 under 510(k) number K923726. 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 DYNAMIC CLIP SYSTEM?

KENSEY NASH DYNAMIC CLIP SYSTEM is a medical device that received FDA 510(k) clearance on 1993-04-06. The listed applicant is Kensey Nash Corp.. The 510(k) number is K923726.

When did KENSEY NASH DYNAMIC CLIP SYSTEM receive FDA 510(k) clearance?

KENSEY NASH DYNAMIC CLIP SYSTEM received FDA 510(k) clearance on 1993-04-06, under 510(k) number K923726.

Who is the listed applicant for KENSEY NASH DYNAMIC CLIP SYSTEM?

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 DYNAMIC CLIP SYSTEM?

The FDA product code for KENSEY NASH DYNAMIC CLIP SYSTEM 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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.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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