meddevicedb.com FDA Device Reference

TUR,ARTHROSCOPIC,CYSTOSCOPY IRRIGATION SETS

K960787 Class II Traditional
Decision Date
1996-05-14
Sponsor / Applicant
Baxter Healthcare Corp

Technical Specification

510(k) Submission ID K960787
Product Code LJH
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 1996-05-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TUR,ARTHROSCOPIC,CYSTOSCOPY IRRIGATION SETS received FDA 510(k) clearance under submission number K960787, sponsored by Baxter Healthcare Corp. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1996-05-14.

Classification & Regulation

This clearance is catalogued under FDA product code LJH and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.