meddevicedb.com FDA Device Reference

ACID BASE LABORATORY ABL4

K833696 Class II Traditional
Decision Date
1984-01-18
Sponsor / Applicant
Radiometer America, Inc.

Technical Specification

510(k) Submission ID K833696
Product Code CEM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1600
Decision Date 1984-01-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACID BASE LABORATORY ABL4 received FDA 510(k) clearance under submission number K833696, sponsored by Radiometer America, 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 1984-01-18.

Classification & Regulation

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