meddevicedb.com FDA Device Reference

DYNACOR STERILE CLOSED SYS. DRAINAGE BAG

K791969 Class II Traditional
Decision Date
1979-11-05
Sponsor / Applicant
Medline Industries, Inc.

Technical Specification

510(k) Submission ID K791969
Product Code KNX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5250
Decision Date 1979-11-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DYNACOR STERILE CLOSED SYS. DRAINAGE BAG received FDA 510(k) clearance under submission number K791969, sponsored by Medline Industries, 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 1979-11-05.

Classification & Regulation

This clearance is catalogued under FDA product code KNX and 21 CFR 876.5250, within the Gastroenterology, Urology review panel as a Class II device.