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REFEREE BRAND CO-OXIMETER REAGENTS

K830180 Class II Traditional
Decision Date
1983-04-08
Sponsor / Applicant
Analytical Products, Inc.

Technical Specification

510(k) Submission ID K830180
Product Code KHG
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7500
Decision Date 1983-04-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REFEREE BRAND CO-OXIMETER REAGENTS received FDA 510(k) clearance under submission number K830180, sponsored by Analytical Products, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1983-04-08.

Classification & Regulation

This clearance is catalogued under FDA product code KHG and 21 CFR 864.7500, within the Hematology review panel as a Class II device.