meddevicedb.com FDA Device Reference

FIBRA SONICS ULTRASONIC LITHOTRIPTOR LITHOSONIC, MODEL LS-2000

K993046 Class II Traditional
Decision Date
1999-11-22
Sponsor / Applicant
Fibra Sonics, Inc.

Technical Specification

510(k) Submission ID K993046
Product Code FEO
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4480
Decision Date 1999-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FIBRA SONICS ULTRASONIC LITHOTRIPTOR LITHOSONIC, MODEL LS-2000 received FDA 510(k) clearance under submission number K993046, sponsored by Fibra Sonics, Inc.. 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 1999-11-22.

Classification & Regulation

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