meddevicedb.com FDA Device Reference

DATA-ZYME TRIGLYCERIDE PROCEDURE

K780379 Class I Traditional
Decision Date
1978-05-12
Sponsor / Applicant
Data Medical Associates, Inc.

Technical Specification

510(k) Submission ID K780379
Product Code CDT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1705
Decision Date 1978-05-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DATA-ZYME TRIGLYCERIDE PROCEDURE received FDA 510(k) clearance under submission number K780379, sponsored by Data Medical Associates, 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 1978-05-12.

Classification & Regulation

This clearance is catalogued under FDA product code CDT and 21 CFR 862.1705, within the Clinical Chemistry review panel as a Class I device.