FDA 510(k)

MENTOR UNISTENT URETERAL STENT SET

K-Number: K875038 · 1988-03-03

Decision Date1988-03-03

Product CodeFAD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MENTOR UNISTENT URETERAL STENT SET is the device name listed in this FDA 510(k) record. The listed applicant is Mentor Corp.. It received FDA 510(k) clearance on 1988-03-03 under 510(k) number K875038. 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 MENTOR UNISTENT URETERAL STENT SET?

MENTOR UNISTENT URETERAL STENT SET is a medical device that received FDA 510(k) clearance on 1988-03-03. The listed applicant is Mentor Corp.. The 510(k) number is K875038.

When did MENTOR UNISTENT URETERAL STENT SET receive FDA 510(k) clearance?

MENTOR UNISTENT URETERAL STENT SET received FDA 510(k) clearance on 1988-03-03, under 510(k) number K875038.

Who is the listed applicant for MENTOR UNISTENT URETERAL STENT SET?

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

What is the FDA product code for MENTOR UNISTENT URETERAL STENT SET?

The FDA product code for MENTOR UNISTENT URETERAL STENT SET is FAD.

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Other records listing Mentor Corp. as applicant

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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.