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QUANTA LITE RNA POL III ELISA

K070066 Class II Traditional
Decision Date
2007-04-11
Sponsor / Applicant
Inova Diagnostics, Inc.

Technical Specification

510(k) Submission ID K070066
Product Code NYO
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 2007-04-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUANTA LITE RNA POL III ELISA received FDA 510(k) clearance under submission number K070066, 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 2007-04-11.

Classification & Regulation

This clearance is catalogued under FDA product code NYO and 21 CFR 866.5100, within the Immunology review panel as a Class II device.