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CYSTO-URETHROSCOPES E-LINE EXISTING OF: SHEATHS, OBTURATORS, INSERTS, ATTCHEMENTS, AND FORCEPS MODEL 8650, 8652, 8660

K011496 Class II Traditional
Decision Date
2001-08-10
Sponsor / Applicant
Richard Wolf Medical Instruments Corp.

Technical Specification

510(k) Submission ID K011496
Product Code FBO
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2001-08-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CYSTO-URETHROSCOPES E-LINE EXISTING OF: SHEATHS, OBTURATORS, INSERTS, ATTCHEMENTS, AND FORCEPS MODEL 8650, 8652, 8660 received FDA 510(k) clearance under submission number K011496, sponsored by Richard Wolf Medical Instruments 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 2001-08-10.

Classification & Regulation

This clearance is catalogued under FDA product code FBO and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.