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ABL555 BLOOD GAS, ELECTROLYTE & METABOLITE SYSTEM

K974818 Class II Traditional
Decision Date
1998-01-16
Sponsor / Applicant
Radiometer America, Inc.

Technical Specification

510(k) Submission ID K974818
Product Code MMI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1215
Decision Date 1998-01-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ABL555 BLOOD GAS, ELECTROLYTE & METABOLITE SYSTEM received FDA 510(k) clearance under submission number K974818, 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 1998-01-16.

Classification & Regulation

This clearance is catalogued under FDA product code MMI and 21 CFR 862.1215, within the Clinical Chemistry review panel as a Class II device.