meddevicedb.com FDA Device Reference

ENEMA BAG

K780877 Class I Traditional
Decision Date
1978-08-14
Sponsor / Applicant
Abco Dealers, Inc.

Technical Specification

510(k) Submission ID K780877
Product Code FCE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5210
Decision Date 1978-08-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENEMA BAG received FDA 510(k) clearance under submission number K780877, sponsored by Abco Dealers, 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 1978-08-14.

Classification & Regulation

This clearance is catalogued under FDA product code FCE and 21 CFR 876.5210, within the Gastroenterology, Urology review panel as a Class I device.