meddevicedb.com FDA Device Reference

GLUCOSE HEXOKINASE COIL REAGENT SYSTEM

K791760 Class II Traditional
Decision Date
1979-09-27
Sponsor / Applicant
Fisher Scientific Co., LLC

Technical Specification

510(k) Submission ID K791760
Product Code CFR
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 1979-09-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GLUCOSE HEXOKINASE COIL REAGENT SYSTEM received FDA 510(k) clearance under submission number K791760, sponsored by Fisher Scientific Co., LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1979-09-27.

Classification & Regulation

This clearance is catalogued under FDA product code CFR and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.