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TECHNICON IMMUNO 1 TM SYSTEM ADDITIONAL ANALYTES

K912616 Class II Traditional
Decision Date
1991-09-25
Sponsor / Applicant
Technicon Instruments Corp.

Technical Specification

510(k) Submission ID K912616
Product Code KLI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1700
Decision Date 1991-09-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TECHNICON IMMUNO 1 TM SYSTEM ADDITIONAL ANALYTES received FDA 510(k) clearance under submission number K912616, sponsored by Technicon Instruments Corp.. 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 1991-09-25.

Classification & Regulation

This clearance is catalogued under FDA product code KLI and 21 CFR 862.1700, within the Clinical Chemistry review panel as a Class II device.