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GOAT ANTI-HUMAN IGM H CHAIN

K832259 Class II Traditional
Decision Date
1983-10-28
Sponsor / Applicant
Gelco Diagnostics, Inc.

Technical Specification

510(k) Submission ID K832259
Product Code DFT
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5550
Decision Date 1983-10-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GOAT ANTI-HUMAN IGM H CHAIN received FDA 510(k) clearance under submission number K832259, sponsored by Gelco Diagnostics, 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 1983-10-28.

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.