FDA 510(k)

BARD TIGERTAIL URETERAL CATHETER

K-Number: K033719 · 2004-02-04

Decision Date2004-02-04

Product CodeKOD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

BARD TIGERTAIL URETERAL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2004-02-04 under 510(k) number K033719. 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 BARD TIGERTAIL URETERAL CATHETER?

BARD TIGERTAIL URETERAL CATHETER is a medical device that received FDA 510(k) clearance on 2004-02-04. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K033719.

When did BARD TIGERTAIL URETERAL CATHETER receive FDA 510(k) clearance?

BARD TIGERTAIL URETERAL CATHETER received FDA 510(k) clearance on 2004-02-04, under 510(k) number K033719.

Who is the listed applicant for BARD TIGERTAIL URETERAL CATHETER?

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

What is the FDA product code for BARD TIGERTAIL URETERAL CATHETER?

The FDA product code for BARD TIGERTAIL URETERAL CATHETER is KOD.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.