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FDA 510(k)

VACCESS FEMORAL CANNULA

K-Number: K842864 · 1984-08-08

ApplicantVas-Cath of Canada , Ltd.
Decision Date1984-08-08
Product CodeKNZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VACCESS FEMORAL CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Vas-Cath of Canada , Ltd.. It received FDA 510(k) clearance on 1984-08-08 under 510(k) number K842864. The device is classified under product code KNZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACCESS FEMORAL CANNULA?

VACCESS FEMORAL CANNULA is a medical device that received FDA 510(k) clearance on 1984-08-08. The listed applicant is Vas-Cath of Canada , Ltd.. The 510(k) number is K842864.

When did VACCESS FEMORAL CANNULA receive FDA 510(k) clearance?

VACCESS FEMORAL CANNULA received FDA 510(k) clearance on 1984-08-08, under 510(k) number K842864.

Who is the listed applicant for VACCESS FEMORAL CANNULA?

The FDA 510(k) record lists Vas-Cath of Canada , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VACCESS FEMORAL CANNULA?

The FDA product code for VACCESS FEMORAL CANNULA is KNZ.

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.

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Other records listing Vas-Cath of Canada , 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.

K875188LUER LOCK CONNECTORS / RIDIG P.V.C.K871817VAS-CATH PERITONEAL DIALYSIS CATHETERK871487VAS-CATH PERMANENT SINGLE LUMEN HEMODIALYSIS CATHK871488VAS-CATH PERMANENT DUAL LUMEN HEMODIALYSIS CATHK863982VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAYK853283VACCESS TM 4006

View all 19 devices →

Related Devices (Code: KNZ)

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.

K842039ARGON DUAL LUMEN HEMODIALYSIS, CATHETERArgon Medical Corp.K844612ACUTE HEMODIALYSIS TRAYSPackaging Technologies, Inc.K842416DUO FLOW CATHETER-MC 54Medical Components, Inc.K841530DOUBLE LUMEN SUBLCAVIAN-FEMORALMedical Components, Inc.K841119TOPS DISPOS. INFUSION SET/HEMODIALYSISTop Surgical Manufacturers Co.K840424HEMOCATH REPAIR KITQuinton, 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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