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PELICALSS HUMAN IGG SUBCLASS NEPHLOMETRIC ARRAY KIT

K982023 Class I Traditional
Decision Date
1998-09-04
Sponsor / Applicant
Inova Diagnostics, Inc.

Technical Specification

510(k) Submission ID K982023
Product Code DAS
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5530
Decision Date 1998-09-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PELICALSS HUMAN IGG SUBCLASS NEPHLOMETRIC ARRAY KIT received FDA 510(k) clearance under submission number K982023, sponsored by Inova 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 1998-09-04.

Classification & Regulation

This clearance is catalogued under FDA product code DAS and 21 CFR 866.5530, within the Immunology review panel as a Class I device.