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IRMA BLOOD ANALYSIS SYSTEM

K945240 Class II Traditional
Decision Date
1995-01-05
Sponsor / Applicant
Diametrics Medical, Inc.

Technical Specification

510(k) Submission ID K945240
Product Code CHL
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1120
Decision Date 1995-01-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IRMA BLOOD ANALYSIS SYSTEM received FDA 510(k) clearance under submission number K945240, sponsored by Diametrics Medical, 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 1995-01-05.

Classification & Regulation

This clearance is catalogued under FDA product code CHL and 21 CFR 862.1120, within the Clinical Chemistry review panel as a Class II device.