meddevicedb.com FDA Device Reference

LIPASE HYDROLYSIS/GLYCEROL KINASE, TRIGLYCERIDES

K863874 Class I Traditional
Decision Date
1986-11-13
Sponsor / Applicant
Electro-Nucleonics Laboratories, Inc.

Technical Specification

510(k) Submission ID K863874
Product Code CDT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1705
Decision Date 1986-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIPASE HYDROLYSIS/GLYCEROL KINASE, TRIGLYCERIDES received FDA 510(k) clearance under submission number K863874, sponsored by Electro-Nucleonics Laboratories, 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 1986-11-13.

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.