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EVA EMPTY SOLUTION CONTAINER W/3 LEAD TRANSFER SET

K890094 Class II Traditional
Decision Date
1989-05-24
Sponsor / Applicant
Kells Medical, Inc.

Technical Specification

510(k) Submission ID K890094
Product Code KPE
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5025
Decision Date 1989-05-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EVA EMPTY SOLUTION CONTAINER W/3 LEAD TRANSFER SET received FDA 510(k) clearance under submission number K890094, sponsored by Kells Medical, 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 1989-05-24.

Classification & Regulation

This clearance is catalogued under FDA product code KPE and 21 CFR 880.5025, within the General Hospital review panel as a Class II device.