meddevicedb.com FDA Device Reference

ELDONCARD

K790282 Class II Traditional
Decision Date
1979-05-04
Sponsor / Applicant
Nordisk Infuser System

Technical Specification

510(k) Submission ID K790282
Product Code KSZ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.9175
Decision Date 1979-05-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELDONCARD received FDA 510(k) clearance under submission number K790282, sponsored by Nordisk Infuser System. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1979-05-04.

Classification & Regulation

This clearance is catalogued under FDA product code KSZ and 21 CFR 864.9175, within the Hematology review panel as a Class II device.