FDA 510(k)

KAMINSKY COMBINATION STENT & INJECTION CATHETER

K-Number: K865085 · 1987-03-25

Decision Date1987-03-25

Product CodeFAD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

KAMINSKY COMBINATION STENT & INJECTION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Van-Tec, Inc.. It received FDA 510(k) clearance on 1987-03-25 under 510(k) number K865085. 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 KAMINSKY COMBINATION STENT & INJECTION CATHETER?

KAMINSKY COMBINATION STENT & INJECTION CATHETER is a medical device that received FDA 510(k) clearance on 1987-03-25. The listed applicant is Van-Tec, Inc.. The 510(k) number is K865085.

When did KAMINSKY COMBINATION STENT & INJECTION CATHETER receive FDA 510(k) clearance?

KAMINSKY COMBINATION STENT & INJECTION CATHETER received FDA 510(k) clearance on 1987-03-25, under 510(k) number K865085.

Who is the listed applicant for KAMINSKY COMBINATION STENT & INJECTION CATHETER?

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

What is the FDA product code for KAMINSKY COMBINATION STENT & INJECTION CATHETER?

The FDA product code for KAMINSKY COMBINATION STENT & INJECTION CATHETER is FAD.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Van-Tec, Inc. as applicant

K880096VAN-TEC ASPIRATION BIOPSY SYSTEM W/COLLECTION CUP K880095BERGER PROSTATE CULTURE CYTOLOGY BRUSH K880098VAN-TEC AUTO BIOPSY NEEDLE K880099VAN-TEC BLADDER EVACUATOR K880094VAN-TEC ENDOPYELOTOMY KNIFE K874112VAN-TEC DOUBLE OCCLUSION BALLOON CATHETER

View all 52 devices →

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.