meddevicedb.com FDA Device Reference

IMMUNOCAP ALLERGEN D201, HOUSE DUST MITE, MODEL 4-4896-01

K092050 Class II Traditional
Decision Date
2009-11-20
Sponsor / Applicant
Phadia AB

Technical Specification

510(k) Submission ID K092050
Product Code DHB
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5750
Decision Date 2009-11-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMMUNOCAP ALLERGEN D201, HOUSE DUST MITE, MODEL 4-4896-01 received FDA 510(k) clearance under submission number K092050, sponsored by Phadia AB. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2009-11-20.

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.