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FDA 510(k)

APPLIED URETERAL CATHETER

K-Number: K020577 · 2002-05-22

ApplicantApplied Medical Resources Corp.
Decision Date2002-05-22
Product CodeEYB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

APPLIED URETERAL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Resources Corp.. It received FDA 510(k) clearance on 2002-05-22 under 510(k) number K020577. The device is classified under product code EYB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APPLIED URETERAL CATHETER?

APPLIED URETERAL CATHETER is a medical device that received FDA 510(k) clearance on 2002-05-22. The listed applicant is Applied Medical Resources Corp.. The 510(k) number is K020577.

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

APPLIED URETERAL CATHETER received FDA 510(k) clearance on 2002-05-22, under 510(k) number K020577.

Who is the listed applicant for APPLIED URETERAL CATHETER?

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

What is the FDA product code for APPLIED URETERAL CATHETER?

The FDA product code for APPLIED URETERAL CATHETER is EYB.

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Related Devices (Code: EYB)

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K192183RocaTub Ureteral CatheterPromepal SamK191187Dornier MINNOW Ureteral CatheterDornier Medtech America, Inc.K183323UPJ Occlusion Balloon CatheterCook IncorporatedK182695Pigtail Ureteral Catheter Set, Sof-Flex AQ Coated Pigtail Ureteral CatheterCook IncorporatedK182122Ureteric CathetersColoplast Corp.K180182Dual Lumen Ureteral Access Catheter, Flexi-Tip Dual Lumen Ureteral Access CatheterCook Incorporated

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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