meddevicedb.com FDA Device Reference

EXP 600 PARALLEL PLATE DIALYZER

K811440 Class II Traditional
Decision Date
1981-06-12
Sponsor / Applicant
Extracorporeal Medical Specialities, Inc.

Technical Specification

510(k) Submission ID K811440
Product Code FJG
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1981-06-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXP 600 PARALLEL PLATE DIALYZER received FDA 510(k) clearance under submission number K811440, sponsored by Extracorporeal Medical Specialities, 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 1981-06-12.

Classification & Regulation

This clearance is catalogued under FDA product code FJG and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.