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SUCTION PUMP FOR INTRACORPOREAL ULTRASOUND LITHOTRIPTER AND ACCESSORIES, MODEL 2207.XXX

K011911 Class II Traditional
Decision Date
2001-09-17
Sponsor / Applicant
Richard Wolf Medical Instruments Corp.

Technical Specification

510(k) Submission ID K011911
Product Code FFK
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4480
Decision Date 2001-09-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUCTION PUMP FOR INTRACORPOREAL ULTRASOUND LITHOTRIPTER AND ACCESSORIES, MODEL 2207.XXX received FDA 510(k) clearance under submission number K011911, 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 2001-09-17.

Classification & Regulation

This clearance is catalogued under FDA product code FFK and 21 CFR 876.4480, within the Gastroenterology, Urology review panel as a Class II device.