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TRICAT RIA (ADRENALIN/NORADRENALIN/DOPAMINE); KATCOMBI RIA (ADRENALIN/NORADRENALIN); NORADRENALIN RIA

K051969 Class I Traditional
Decision Date
2005-10-03
Sponsor / Applicant
Ibl GmbH

Technical Specification

510(k) Submission ID K051969
Product Code CHQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1165
Decision Date 2005-10-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRICAT RIA (ADRENALIN/NORADRENALIN/DOPAMINE); KATCOMBI RIA (ADRENALIN/NORADRENALIN); NORADRENALIN RIA received FDA 510(k) clearance under submission number K051969, sponsored by Ibl GmbH. 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 2005-10-03.

Classification & Regulation

This clearance is catalogued under FDA product code CHQ and 21 CFR 862.1165, within the Clinical Chemistry review panel as a Class I device.