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FDA 510(k)

PANAMEX(TM) URETERAL STENT

K-Number: K882157 · 1988-08-02

ApplicantKingston Technologies, Inc.
Decision Date1988-08-02
Product CodeFAD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PANAMEX(TM) URETERAL STENT is the device name listed in this FDA 510(k) record. The listed applicant is Kingston Technologies, Inc.. It received FDA 510(k) clearance on 1988-08-02 under 510(k) number K882157. 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 PANAMEX(TM) URETERAL STENT?

PANAMEX(TM) URETERAL STENT is a medical device that received FDA 510(k) clearance on 1988-08-02. The listed applicant is Kingston Technologies, Inc.. The 510(k) number is K882157.

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

PANAMEX(TM) URETERAL STENT received FDA 510(k) clearance on 1988-08-02, under 510(k) number K882157.

Who is the listed applicant for PANAMEX(TM) URETERAL STENT?

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

What is the FDA product code for PANAMEX(TM) URETERAL STENT?

The FDA product code for PANAMEX(TM) URETERAL STENT is FAD.

Related Clinical Trials

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Other records listing Kingston Technologies, Inc. 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.

K935232HYDROTORQUE GUIDE WIREK940814HYDRO-M(TM) WOUND GELK940738KTI HY-Q(TM) WOUND DRESSINGK925660KTI TRANSPARENT WOUND DRESSINGK921502HYSORB WOUND DRESSING

Related Devices (Code: FAD)

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.

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 CorporationK232920RELIEF™ 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

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

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