meddevicedb.com FDA Device Reference

IMMUNOCAP ALLERGEN K82

K121463 Class II Traditional
Decision Date
2013-01-29
Sponsor / Applicant
Thermo Fisher Scientific

Technical Specification

510(k) Submission ID K121463
Product Code DHB
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5750
Decision Date 2013-01-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMMUNOCAP ALLERGEN K82 received FDA 510(k) clearance under submission number K121463, sponsored by Thermo Fisher Scientific. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2013-01-29.

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.