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FDA 510(k)

HEMOFILTRATION CATHETER HF-100

K-Number: K840322 · 1984-04-24

ApplicantVas-Cath of Canada , Ltd.
Decision Date1984-04-24
Product CodeFIQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HEMOFILTRATION CATHETER HF-100 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 1984-04-24 under 510(k) number K840322. 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 HEMOFILTRATION CATHETER HF-100?

HEMOFILTRATION CATHETER HF-100 is a medical device that received FDA 510(k) clearance on 1984-04-24. The listed applicant is Vas-Cath of Canada , Ltd.. The 510(k) number is K840322.

When did HEMOFILTRATION CATHETER HF-100 receive FDA 510(k) clearance?

HEMOFILTRATION CATHETER HF-100 received FDA 510(k) clearance on 1984-04-24, under 510(k) number K840322.

Who is the listed applicant for HEMOFILTRATION CATHETER HF-100?

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 HEMOFILTRATION CATHETER HF-100?

The FDA product code for HEMOFILTRATION CATHETER HF-100 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 CATHETERK871487VAS-CATH PERMANENT SINGLE LUMEN HEMODIALYSIS CATHK871488VAS-CATH PERMANENT DUAL 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.K840415HEMOCATHQuinton, 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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