meddevicedb.com FDA Device Reference

SCB/VALLEYLAB FORCE FX INTERFACE UNIT

K041912 Class II Traditional
Decision Date
2004-10-25
Sponsor / Applicant
KARL STORZ Endoscopy-America, Inc.

Technical Specification

510(k) Submission ID K041912
Product Code ODA
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2004-10-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SCB/VALLEYLAB FORCE FX INTERFACE UNIT received FDA 510(k) clearance under submission number K041912, sponsored by KARL STORZ Endoscopy-America, 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 2004-10-25.

Classification & Regulation

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