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ENEMA BUCKET SET

K901179 Class I Traditional
Decision Date
1990-06-28
Sponsor / Applicant
Orion Life Systems, Inc.

Technical Specification

510(k) Submission ID K901179
Product Code FCE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5210
Decision Date 1990-06-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENEMA BUCKET SET received FDA 510(k) clearance under submission number K901179, sponsored by Orion Life Systems, 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 1990-06-28.

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.