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SEROTONIN ENZYME IMMUNOASSAY

K903609 Class I Traditional
Decision Date
1990-10-22
Sponsor / Applicant
Immunotech Corp.

Technical Specification

510(k) Submission ID K903609
Product Code CDA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1390
Decision Date 1990-10-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SEROTONIN ENZYME IMMUNOASSAY received FDA 510(k) clearance under submission number K903609, sponsored by Immunotech 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 1990-10-22.

Classification & Regulation

This clearance is catalogued under FDA product code CDA and 21 CFR 862.1390, within the Clinical Chemistry review panel as a Class I device.