meddevicedb.com FDA Device Reference

FLUID CONTROL

K982117 Class I Traditional
Decision Date
1998-09-04
Sponsor / Applicant
T.A. Coleman Ent.

Technical Specification

510(k) Submission ID K982117
Product Code EIA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6640
Decision Date 1998-09-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLUID CONTROL received FDA 510(k) clearance under submission number K982117, sponsored by T.A. Coleman Ent.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1998-09-04.

Classification & Regulation

This clearance is catalogued under FDA product code EIA and 21 CFR 872.6640, within the Dental review panel as a Class I device.