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FDA 510(k)

PARALLEL DUAL LUMEN SUBCLAVIAN CANNULA

K-Number: K834358 · 1984-04-02

ApplicantVas-Cath of Canada , Ltd.
Decision Date1984-04-02
Product CodeFIQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PARALLEL DUAL 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 1984-04-02 under 510(k) number K834358. The device is classified under product code FIQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARALLEL DUAL LUMEN SUBCLAVIAN CANNULA?

PARALLEL DUAL LUMEN SUBCLAVIAN CANNULA is a medical device that received FDA 510(k) clearance on 1984-04-02. The listed applicant is Vas-Cath of Canada , Ltd.. The 510(k) number is K834358.

When did PARALLEL DUAL LUMEN SUBCLAVIAN CANNULA receive FDA 510(k) clearance?

PARALLEL DUAL LUMEN SUBCLAVIAN CANNULA received FDA 510(k) clearance on 1984-04-02, under 510(k) number K834358.

Who is the listed applicant for PARALLEL DUAL 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 PARALLEL DUAL LUMEN SUBCLAVIAN CANNULA?

The FDA product code for PARALLEL DUAL LUMEN SUBCLAVIAN CANNULA is FIQ.

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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 CATHETERK871488VAS-CATH PERMANENT DUAL LUMEN HEMODIALYSIS CATHK871487VAS-CATH PERMANENT SINGLE LUMEN HEMODIALYSIS CATHK863982VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAYK853283VACCESS TM 4006

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Related Devices (Code: FIQ)

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.

K892887ST SERIES SAF-T-SHUNTS ARTERIOVENOUS CANNULAAkcess Medical Products, Inc.K892663S-100 ALLEN-BROWN SHUNTAkcess Medical Products, Inc.K892666SAF-T-SHUNT, S-300 SERIESAkcess Medical Products, Inc.K844692PEDIATRIC SIZED HEMOCATH CATHETERQuinton, Inc.K841791PLUME FISTULA NEEDLEHospal Medical Corp.K840322HEMOFILTRATION CATHETER HF-100Vas-Cath of Canada , Ltd.

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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