meddevicedb.com FDA Device Reference

ENDOSCOPIC APPLICATOR

K120608 Class II Traditional
Decision Date
2012-03-15
Sponsor / Applicant
Micromedics, Inc.

Technical Specification

510(k) Submission ID K120608
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2012-03-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDOSCOPIC APPLICATOR received FDA 510(k) clearance under submission number K120608, sponsored by Micromedics, 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 2012-03-15.

Classification & Regulation

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