FDA 510(k)

PEDIATRIC URETERAL STENT

K-Number: K060673 · 2006-03-29

ApplicantApplied Medical Resources Corp.

Decision Date2006-03-29

Product CodeFAD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

PEDIATRIC URETERAL STENT 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 2006-03-29 under 510(k) number K060673. The device is classified under product code FAD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDIATRIC URETERAL STENT?

PEDIATRIC URETERAL STENT is a medical device that received FDA 510(k) clearance on 2006-03-29. The listed applicant is Applied Medical Resources Corp.. The 510(k) number is K060673.

When did PEDIATRIC URETERAL STENT receive FDA 510(k) clearance?

PEDIATRIC URETERAL STENT received FDA 510(k) clearance on 2006-03-29, under 510(k) number K060673.

Who is the listed applicant for PEDIATRIC URETERAL STENT?

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 PEDIATRIC URETERAL STENT?

The FDA product code for PEDIATRIC URETERAL STENT is FAD.

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Related Devices (Code: FAD)

K251890Disposable Ureteral StentsZhejiang Chuangxiang Medical Technology Co., Ltd.K251469Endura™ Ureteral Stent and Stent SetCathegenix (Xiamen) Co., Ltd.K243039Ureteral Stents (AF-D series)Alton (Shanghai) Medical Instruments Co., Ltd.K243830Disposable ureteral stentShenzhen Trious Medical Technology Co., Ltd.K250824Percuflex Ureteral Stent; Percuflex Plus Ureteral Stent; Percuflex Plus SureDrive Steerable Ureteral Stent Set; Contour Ureteral Stent; Contour SureDrive Steerable Ureteral Stent Set; Contour VL Variable Length Ureteral Stent; Contour VL SureDrive Steerable Ureteral Stent Set; Polaris Ultra Ureteral Stent; Polaris Loop Ureteral Stent; Tria Firm Ureteral Stent; Tria Soft Ureteral Stent; Percuflex Urinary Diversion Stent SetBoston Scientific Corporation K232920RELIEF™ Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF™ Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cmUreteral Stent Company

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.