meddevicedb.com FDA Device Reference

BIURET REAGENT & TOTAL PROTEIN BLANK SOL

K802161 Class II Traditional
Decision Date
1980-10-10
Sponsor / Applicant
Panmed, Inc.

Technical Specification

510(k) Submission ID K802161
Product Code CEK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1635
Decision Date 1980-10-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIURET REAGENT & TOTAL PROTEIN BLANK SOL received FDA 510(k) clearance under submission number K802161, sponsored by Panmed, Inc.. 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 1980-10-10.

Classification & Regulation

This clearance is catalogued under FDA product code CEK and 21 CFR 862.1635, within the Clinical Chemistry review panel as a Class II device.