meddevicedb.com FDA Device Reference

EASY-TEST POTASSIUM K ITEM NUMBER 19XXX

K880339 Class II Traditional
Decision Date
1988-02-25
Sponsor / Applicant
Em Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K880339
Product Code CEJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1600
Decision Date 1988-02-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EASY-TEST POTASSIUM K ITEM NUMBER 19XXX received FDA 510(k) clearance under submission number K880339, sponsored by Em Diagnostic Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1988-02-25.

Classification & Regulation

This clearance is catalogued under FDA product code CEJ and 21 CFR 862.1600, within the Clinical Chemistry review panel as a Class II device.