meddevicedb.com FDA Device Reference

ULTRACHEM E-GLU, #64976 & 65040

K821461 Class II Traditional
Decision Date
1982-06-02
Sponsor / Applicant
Emd Chemicals, Inc.

Technical Specification

510(k) Submission ID K821461
Product Code CFR
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 1982-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTRACHEM E-GLU, #64976 & 65040 received FDA 510(k) clearance under submission number K821461, sponsored by Emd Chemicals, 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 1982-06-02.

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.