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FDA 510(k)

VACCESS 2000 SINGLE LUMEN SUBCLAVIAN CANNULA

K-Number: K844433 · 1985-03-13

ApplicantVas-Cath of Canada , Ltd.
Decision Date1985-03-13
Product CodeLFJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VACCESS 2000 SINGLE LUMEN SUBCLAVIAN 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 1985-03-13 under 510(k) number K844433. The device is classified under product code LFJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACCESS 2000 SINGLE LUMEN SUBCLAVIAN CANNULA?

VACCESS 2000 SINGLE LUMEN SUBCLAVIAN CANNULA is a medical device that received FDA 510(k) clearance on 1985-03-13. The listed applicant is Vas-Cath of Canada , Ltd.. The 510(k) number is K844433.

When did VACCESS 2000 SINGLE LUMEN SUBCLAVIAN CANNULA receive FDA 510(k) clearance?

VACCESS 2000 SINGLE LUMEN SUBCLAVIAN CANNULA received FDA 510(k) clearance on 1985-03-13, under 510(k) number K844433.

Who is the listed applicant for VACCESS 2000 SINGLE LUMEN SUBCLAVIAN 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 2000 SINGLE LUMEN SUBCLAVIAN CANNULA?

The FDA product code for VACCESS 2000 SINGLE LUMEN SUBCLAVIAN CANNULA is LFJ.

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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: LFJ)

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.

K920780MEDSURG INSERTION TRAYMedsurg Industries, Inc.K925819AKCESS0CATH KITAkcess Medical Products, Inc.K925818AKCESS-CATHAkcess Medical Products, Inc.K913468ULDALL DOUBLE LUMEN HEMODIALYSIS CATHETER SET/TRAYCook, Inc.K931120COAXIAL ACUTE CATHETERAkcess Medical Products, Inc.K920634SPLITTABLE SHEATH INTRODUCER SETAkcess Medical Products, 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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