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NOVA STAT PROFILE PHOX ULTRA ANALYZER SYSTEM

K110648 Class II Special
Decision Date
2011-08-29
Sponsor / Applicant
Nova Biomedical Corporation

Technical Specification

510(k) Submission ID K110648
Product Code CHL
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1120
Decision Date 2011-08-29
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NOVA STAT PROFILE PHOX ULTRA ANALYZER SYSTEM received FDA 510(k) clearance under submission number K110648, sponsored by Nova Biomedical Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2011-08-29.

Classification & Regulation

This clearance is catalogued under FDA product code CHL and 21 CFR 862.1120, within the Clinical Chemistry review panel as a Class II device.