meddevicedb.com FDA Device Reference

ELM ALLERGEN DISC

K863973 Class II Traditional
Decision Date
1986-12-01
Sponsor / Applicant
Immuno Nuclear Corp.

Technical Specification

510(k) Submission ID K863973
Product Code DHB
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5750
Decision Date 1986-12-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELM ALLERGEN DISC received FDA 510(k) clearance under submission number K863973, sponsored by Immuno Nuclear Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1986-12-01.

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.