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FDA 510(k)

14F DUAL FLOATING DIALYSIS CATHETER/TRAY

K-Number: K042672 · 2005-03-23

ApplicantCardio Med Supplies, Inc.
Decision Date2005-03-23
Product CodeMSD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

14F DUAL FLOATING DIALYSIS CATHETER/TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Cardio Med Supplies, Inc.. It received FDA 510(k) clearance on 2005-03-23 under 510(k) number K042672. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 14F DUAL FLOATING DIALYSIS CATHETER/TRAY?

14F DUAL FLOATING DIALYSIS CATHETER/TRAY is a medical device that received FDA 510(k) clearance on 2005-03-23. The listed applicant is Cardio Med Supplies, Inc.. The 510(k) number is K042672.

When did 14F DUAL FLOATING DIALYSIS CATHETER/TRAY receive FDA 510(k) clearance?

14F DUAL FLOATING DIALYSIS CATHETER/TRAY received FDA 510(k) clearance on 2005-03-23, under 510(k) number K042672.

Who is the listed applicant for 14F DUAL FLOATING DIALYSIS CATHETER/TRAY?

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

What is the FDA product code for 14F DUAL FLOATING DIALYSIS CATHETER/TRAY?

The FDA product code for 14F DUAL FLOATING DIALYSIS CATHETER/TRAY is MSD.

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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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