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FDA 510(k)

NEXTSTEP ANTEGRADE CHRONIC HEMODIALYSIS CATHETER

K-Number: K111900 · 2011-08-17

ApplicantTeleflexmedical, Inc.
Decision Date2011-08-17
Product CodeMSD
Advisory CommitteeGU
DecisionUnknown

Device Summary

NEXTSTEP ANTEGRADE CHRONIC HEMODIALYSIS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Teleflexmedical, Inc.. It received FDA 510(k) clearance on 2011-08-17 under 510(k) number K111900. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the NEXTSTEP ANTEGRADE CHRONIC HEMODIALYSIS CATHETER?

NEXTSTEP ANTEGRADE CHRONIC HEMODIALYSIS CATHETER is a medical device that received FDA 510(k) clearance on 2011-08-17. The listed applicant is Teleflexmedical, Inc.. The 510(k) number is K111900.

When did NEXTSTEP ANTEGRADE CHRONIC HEMODIALYSIS CATHETER receive FDA 510(k) clearance?

NEXTSTEP ANTEGRADE CHRONIC HEMODIALYSIS CATHETER received FDA 510(k) clearance on 2011-08-17, under 510(k) number K111900.

Who is the listed applicant for NEXTSTEP ANTEGRADE CHRONIC HEMODIALYSIS CATHETER?

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

What is the FDA product code for NEXTSTEP ANTEGRADE CHRONIC HEMODIALYSIS CATHETER?

The FDA product code for NEXTSTEP ANTEGRADE CHRONIC HEMODIALYSIS CATHETER is MSD.

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Related Devices (Code: MSD)

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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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