meddevicedb.com FDA Device Reference

AIA-PACK TPOAB ASSAY

K981521 Class II Traditional
Decision Date
1998-10-08
Sponsor / Applicant
Tosoh Medics, Inc.

Technical Specification

510(k) Submission ID K981521
Product Code JZO
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5870
Decision Date 1998-10-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AIA-PACK TPOAB ASSAY received FDA 510(k) clearance under submission number K981521, sponsored by Tosoh Medics, 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 1998-10-08.

Classification & Regulation

This clearance is catalogued under FDA product code JZO and 21 CFR 866.5870, within the Immunology review panel as a Class II device.