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SUCROSEP SPECIFIC IMMUNORADIOMETRIC ASSAY

K880758 Class I Traditional
Decision Date
1988-04-18
Sponsor / Applicant
Boots-Celltech Diagnostics, Inc.

Technical Specification

510(k) Submission ID K880758
Product Code CEP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1485
Decision Date 1988-04-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUCROSEP SPECIFIC IMMUNORADIOMETRIC ASSAY received FDA 510(k) clearance under submission number K880758, sponsored by Boots-Celltech Diagnostics, Inc.. 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 1988-04-18.

Classification & Regulation

This clearance is catalogued under FDA product code CEP and 21 CFR 862.1485, within the Clinical Chemistry review panel as a Class I device.