meddevicedb.com FDA Device Reference

S*E*M*M-SET & C*U*R*T-SET

K932617 Class II Traditional
Decision Date
1994-03-07
Sponsor / Applicant
Market-Tiers, Inc.

Technical Specification

510(k) Submission ID K932617
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1994-03-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

S*E*M*M-SET & C*U*R*T-SET received FDA 510(k) clearance under submission number K932617, sponsored by Market-Tiers, 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 1994-03-07.

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.