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PHADEZYM IGE PRIST TEST

K810507 Class II Traditional
Decision Date
1981-03-20
Sponsor / Applicant
Pharmacia, Inc.

Technical Specification

510(k) Submission ID K810507
Product Code DGC
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 1981-03-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHADEZYM IGE PRIST TEST received FDA 510(k) clearance under submission number K810507, 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 1981-03-20.

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.