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DRAINAGE BAG

K990428 Class II Traditional
Decision Date
1999-08-12
Sponsor / Applicant
Remington Medical, Inc.

Technical Specification

510(k) Submission ID K990428
Product Code EXF
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5010
Decision Date 1999-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DRAINAGE BAG received FDA 510(k) clearance under submission number K990428, sponsored by Remington Medical, 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 1999-08-12.

Classification & Regulation

This clearance is catalogued under FDA product code EXF and 21 CFR 876.5010, within the Gastroenterology, Urology review panel as a Class II device.