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AMERLIITE FT4 ASSAY LAN.0006/2006 240/144 TEST KIT

K883123 Class II Traditional
Decision Date
1988-12-22
Sponsor / Applicant
Amersham Corp.

Technical Specification

510(k) Submission ID K883123
Product Code CEC
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1695
Decision Date 1988-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AMERLIITE FT4 ASSAY LAN.0006/2006 240/144 TEST KIT received FDA 510(k) clearance under submission number K883123, sponsored by Amersham 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 1988-12-22.

Classification & Regulation

This clearance is catalogued under FDA product code CEC and 21 CFR 862.1695, within the Clinical Chemistry review panel as a Class II device.