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FDA 510(k)

DOVER RED RUBBER ROBINSON CATHETER

K-Number: K041243 · 2004-07-07

ApplicantTyco Healthcare
Decision Date2004-07-07
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DOVER RED RUBBER ROBINSON CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Tyco Healthcare. It received FDA 510(k) clearance on 2004-07-07 under 510(k) number K041243. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOVER RED RUBBER ROBINSON CATHETER?

DOVER RED RUBBER ROBINSON CATHETER is a medical device that received FDA 510(k) clearance on 2004-07-07. The listed applicant is Tyco Healthcare. The 510(k) number is K041243.

When did DOVER RED RUBBER ROBINSON CATHETER receive FDA 510(k) clearance?

DOVER RED RUBBER ROBINSON CATHETER received FDA 510(k) clearance on 2004-07-07, under 510(k) number K041243.

Who is the listed applicant for DOVER RED RUBBER ROBINSON CATHETER?

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

What is the FDA product code for DOVER RED RUBBER ROBINSON CATHETER?

The FDA product code for DOVER RED RUBBER ROBINSON CATHETER is KOD.

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Other records listing Tyco Healthcare 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.

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Related Devices (Code: KOD)

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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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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