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FDA 510(k)

FREKATHETER VENOUS CATHETERISATION SYS

K-Number: K841718 · 1984-04-25

ApplicantFresenius USA, Inc.
Decision Date1984-04-25
Product Code
DecisionUnknown

Device Summary

FREKATHETER VENOUS CATHETERISATION SYS is the device name listed in this FDA 510(k) record. The listed applicant is Fresenius USA, Inc.. It received FDA 510(k) clearance on 1984-04-25 under 510(k) number K841718. FDA Decision: Unknown.

Frequently Asked Questions

What is the FREKATHETER VENOUS CATHETERISATION SYS?

FREKATHETER VENOUS CATHETERISATION SYS is a medical device that received FDA 510(k) clearance on 1984-04-25. The listed applicant is Fresenius USA, Inc.. The 510(k) number is K841718.

When did FREKATHETER VENOUS CATHETERISATION SYS receive FDA 510(k) clearance?

FREKATHETER VENOUS CATHETERISATION SYS received FDA 510(k) clearance on 1984-04-25, under 510(k) number K841718.

Who is the listed applicant for FREKATHETER VENOUS CATHETERISATION SYS?

The FDA 510(k) record lists Fresenius USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Fresenius USA, Inc. 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.

K992275FRESENIUS MODIFIED F400 LOW VOLUME HEMOCONCENTRATOR F3000 & MODIFIED F400 LOW VOL HEMOCONCENTRATOR W/TUBING SET F3000TSK970700FRESENIUS POLYSULFONE HEMODIALYZERS, BOTH LOW AND HIGH FLUXK974584FRESENIUS F SERIES HEMOCONCENTRATORS F400,F500,F700,F800,F400TS,F500TS,F700S,F800TSK973378C.A.T.S CONTINUOUS AUTOTRANSFUSION SYSTEM MODEL 900500 1, AT1 AUTOTRANSFUSION SET MODEL 900 510 1, PSQ SET (DD) MODEL 61K9614652008H ON LINE CLEARANCE MONITORK955762PACKPD PERITONEAL DIALYSIS UREA KINETIC MODELING SOFTWARE PROGRAM

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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