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FDA 510(k)

PALINDROME RT CHRONIC CATHETER

K-Number: K111817 · 2011-08-30

ApplicantCovidien
Decision Date2011-08-30
Product CodeMSD
Advisory CommitteeGU
DecisionUnknown

Device Summary

PALINDROME RT CHRONIC CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Covidien. It received FDA 510(k) clearance on 2011-08-30 under 510(k) number K111817. 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 RT CHRONIC CATHETER?

PALINDROME RT CHRONIC CATHETER is a medical device that received FDA 510(k) clearance on 2011-08-30. The listed applicant is Covidien. The 510(k) number is K111817.

When did PALINDROME RT CHRONIC CATHETER receive FDA 510(k) clearance?

PALINDROME RT CHRONIC CATHETER received FDA 510(k) clearance on 2011-08-30, under 510(k) number K111817.

Who is the listed applicant for PALINDROME RT CHRONIC CATHETER?

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

What is the FDA product code for PALINDROME RT CHRONIC CATHETER?

The FDA product code for PALINDROME RT CHRONIC 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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