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IL PHOENIX, MODEL 900, CHEMISTRY/ELECTROLYTE ANALY

K884771 Class II Traditional
Decision Date
1989-02-10
Sponsor / Applicant
Instrumentation Laboratory CO

Technical Specification

510(k) Submission ID K884771
Product Code JFP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1145
Decision Date 1989-02-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IL PHOENIX, MODEL 900, CHEMISTRY/ELECTROLYTE ANALY received FDA 510(k) clearance under submission number K884771, sponsored by Instrumentation Laboratory CO. 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 1989-02-10.

Classification & Regulation

This clearance is catalogued under FDA product code JFP and 21 CFR 862.1145, within the Clinical Chemistry review panel as a Class II device.