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TECHNICON TESTPOINT(TM) LIGAND CONTROL

K900717 Class I Traditional
Decision Date
1990-04-26
Sponsor / Applicant
Technicon Instruments Corp.

Technical Specification

510(k) Submission ID K900717
Product Code JJY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1990-04-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TECHNICON TESTPOINT(TM) LIGAND CONTROL received FDA 510(k) clearance under submission number K900717, 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 1990-04-26.

Classification & Regulation

This clearance is catalogued under FDA product code JJY and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.