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PHARMACIA IGE EIA ULTRA

K882626 Class II Traditional
Decision Date
1988-08-04
Sponsor / Applicant
Pharmacia, Inc.

Technical Specification

510(k) Submission ID K882626
Product Code DGC
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 1988-08-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHARMACIA IGE EIA ULTRA received FDA 510(k) clearance under submission number K882626, sponsored by Pharmacia, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1988-08-04.

Classification & Regulation

This clearance is catalogued under FDA product code DGC and 21 CFR 866.5510, within the Immunology review panel as a Class II device.