meddevicedb.com FDA Device Reference

ALLERGEN IMMUNOCAP, MODELS C74, E89, EX2, EX70, EX71, EX73, FX8, FX9, FX10, FX16, FX73, I72, I75, I76, K71, K73, K81, K8

K000132 Class II Traditional
Decision Date
2000-02-18
Sponsor / Applicant
Pharmacia & Upjohn Co.

Technical Specification

510(k) Submission ID K000132
Product Code DHB
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5750
Decision Date 2000-02-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALLERGEN IMMUNOCAP, MODELS C74, E89, EX2, EX70, EX71, EX73, FX8, FX9, FX10, FX16, FX73, I72, I75, I76, K71, K73, K81, K8 received FDA 510(k) clearance under submission number K000132, sponsored by Pharmacia & Upjohn Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2000-02-18.

Classification & Regulation

This clearance is catalogued under FDA product code DHB and 21 CFR 866.5750, within the Immunology review panel as a Class II device.