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ROSCH -THURMOND FALLOPIAN TUBE CATHETERIZATION SET

K955508 Class II Traditional
Decision Date
1996-02-26
Sponsor / Applicant
Cook Urological, Inc.

Technical Specification

510(k) Submission ID K955508
Product Code LKF
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4530
Decision Date 1996-02-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ROSCH -THURMOND FALLOPIAN TUBE CATHETERIZATION SET received FDA 510(k) clearance under submission number K955508, sponsored by Cook Urological, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1996-02-26.

Classification & Regulation

This clearance is catalogued under FDA product code LKF and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class II device.