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FDA 510(k)

PALINDROME 14.5 FR CHRONIC HEMODIALYSIS CATHETER

K-Number: K033676 · 2004-02-20

ApplicantKendall
Decision Date2004-02-20
Product CodeMSD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PALINDROME 14.5 FR CHRONIC HEMODIALYSIS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Kendall. It received FDA 510(k) clearance on 2004-02-20 under 510(k) number K033676. 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 PALINDROME 14.5 FR CHRONIC HEMODIALYSIS CATHETER?

PALINDROME 14.5 FR CHRONIC HEMODIALYSIS CATHETER is a medical device that received FDA 510(k) clearance on 2004-02-20. The listed applicant is Kendall. The 510(k) number is K033676.

When did PALINDROME 14.5 FR CHRONIC HEMODIALYSIS CATHETER receive FDA 510(k) clearance?

PALINDROME 14.5 FR CHRONIC HEMODIALYSIS CATHETER received FDA 510(k) clearance on 2004-02-20, under 510(k) number K033676.

Who is the listed applicant for PALINDROME 14.5 FR CHRONIC HEMODIALYSIS CATHETER?

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

What is the FDA product code for PALINDROME 14.5 FR CHRONIC HEMODIALYSIS CATHETER?

The FDA product code for PALINDROME 14.5 FR CHRONIC HEMODIALYSIS CATHETER is MSD.

Related Clinical Trials

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.

Other records listing Kendall 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.

View all 12 devices →

Related Devices (Code: MSD)

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.

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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