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LUNDIA 10-5-L PARRALLE FLOW DIALYZER

K823791 Class II Traditional
Decision Date
1983-01-12
Sponsor / Applicant
Gambro, Inc.

Technical Specification

510(k) Submission ID K823791
Product Code KOC
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1983-01-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LUNDIA 10-5-L PARRALLE FLOW DIALYZER received FDA 510(k) clearance under submission number K823791, sponsored by Gambro, 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 1983-01-12.

Classification & Regulation

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