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IRMA BLOOD ANALYSIS SYSTEM WITH OPTIONAL MULTI-USE CARTRIDGE

K980523 Class II Traditional
Decision Date
1998-03-19
Sponsor / Applicant
Diametrics Medical, Inc.

Technical Specification

510(k) Submission ID K980523
Product Code CHL
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1120
Decision Date 1998-03-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IRMA BLOOD ANALYSIS SYSTEM WITH OPTIONAL MULTI-USE CARTRIDGE received FDA 510(k) clearance under submission number K980523, 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 1998-03-19.

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.