meddevicedb.com FDA Device Reference

CHEMMATE(TM) KAPPA

K950150 Class II Traditional
Decision Date
1995-10-27
Sponsor / Applicant
Biotek Solutions, Inc.

Technical Specification

510(k) Submission ID K950150
Product Code DFH
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5550
Decision Date 1995-10-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHEMMATE(TM) KAPPA received FDA 510(k) clearance under submission number K950150, sponsored by Biotek Solutions, 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 1995-10-27.

Classification & Regulation

This clearance is catalogued under FDA product code DFH and 21 CFR 866.5550, within the Immunology review panel as a Class II device.