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FALLER STYLET

K130441 Class II Traditional
Decision Date
2013-04-19
Sponsor / Applicant
Medionics International, Inc.

Technical Specification

510(k) Submission ID K130441
Product Code FJS
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5630
Decision Date 2013-04-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FALLER STYLET received FDA 510(k) clearance under submission number K130441, sponsored by Medionics International, 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 2013-04-19.

Classification & Regulation

This clearance is catalogued under FDA product code FJS and 21 CFR 876.5630, within the Gastroenterology, Urology review panel as a Class II device.