meddevicedb.com FDA Device Reference

PLEUR-EVAC(R) A-8020--INFANT CHEST DRAINAGE SYSTEM

K890129 Class II Traditional
Decision Date
1989-04-10
Sponsor / Applicant
Deknatel, Inc.

Technical Specification

510(k) Submission ID K890129
Product Code GCX
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6740
Decision Date 1989-04-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PLEUR-EVAC(R) A-8020--INFANT CHEST DRAINAGE SYSTEM received FDA 510(k) clearance under submission number K890129, sponsored by Deknatel, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1989-04-10.

Classification & Regulation

This clearance is catalogued under FDA product code GCX and 21 CFR 880.6740, within the General Hospital review panel as a Class II device.