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FDA 510(k)

PALINDROME P HEMODIALYSIS CATHETER

K-Number: K092205 · 2009-10-30

ApplicantCovidien Lp, Formerly Registered AS Kendall
Decision Date2009-10-30
Product CodeMSD
Advisory CommitteeGU
DecisionUnknown

Device Summary

PALINDROME P HEMODIALYSIS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Covidien Lp, Formerly Registered AS Kendall. It received FDA 510(k) clearance on 2009-10-30 under 510(k) number K092205. 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 PALINDROME P HEMODIALYSIS CATHETER?

PALINDROME P HEMODIALYSIS CATHETER is a medical device that received FDA 510(k) clearance on 2009-10-30. The listed applicant is Covidien Lp, Formerly Registered AS Kendall. The 510(k) number is K092205.

When did PALINDROME P HEMODIALYSIS CATHETER receive FDA 510(k) clearance?

PALINDROME P HEMODIALYSIS CATHETER received FDA 510(k) clearance on 2009-10-30, under 510(k) number K092205.

Who is the listed applicant for PALINDROME P HEMODIALYSIS CATHETER?

The FDA 510(k) record lists Covidien Lp, Formerly Registered AS Kendall as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PALINDROME P HEMODIALYSIS CATHETER?

The FDA product code for PALINDROME P 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.

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Other records listing Covidien Lp, Formerly Registered AS 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.

K130725MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.K112511DOBBHOFF DUAL PORT FEEDING TUBE

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.

K241581Hemodialysis CatheterHaolang Medical USA CorporationK210461End CapMedical Components Inc (Medcomp)K203575GlidePath Retro Long-Term Hemodialysis CatheterC.R. Bard, Inc.K211410GlidePath 13F Long-Term Hemodialysis CatheterBard Peripheral Vascular, Inc.K203767Pristine Long-Term Hemodialysis CatheterC B Bard, Inc.K202150GlidePath 7.5F Long-Term Dialysis CatheterC.R. Bard, Inc.

Official Source

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