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IL TEST 97573-15, PLASMINOGEN ASSAY

K864212 Class I Traditional
Decision Date
1986-12-04
Sponsor / Applicant
Instrumentation Laboratory CO

Technical Specification

510(k) Submission ID K864212
Product Code DDX
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5715
Decision Date 1986-12-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IL TEST 97573-15, PLASMINOGEN ASSAY received FDA 510(k) clearance under submission number K864212, sponsored by Instrumentation Laboratory CO. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1986-12-04.

Classification & Regulation

This clearance is catalogued under FDA product code DDX and 21 CFR 866.5715, within the Immunology review panel as a Class I device.