meddevicedb.com FDA Device Reference

AMER. HISTO-ID SYS PRIMARY IGM S7920-31

K842327 Class II Traditional
Decision Date
1984-08-02
Sponsor / Applicant
Bartels Immunodiagnostic Supplies, Inc.

Technical Specification

510(k) Submission ID K842327
Product Code DFT
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5550
Decision Date 1984-08-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AMER. HISTO-ID SYS PRIMARY IGM S7920-31 received FDA 510(k) clearance under submission number K842327, sponsored by Bartels Immunodiagnostic Supplies, 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 1984-08-02.

Classification & Regulation

This clearance is catalogued under FDA product code DFT and 21 CFR 866.5550, within the Immunology review panel as a Class II device.