meddevicedb.com FDA Device Reference

WAKO L-TYPE TRIGLYCERIDE TEST

K993466 Class I Traditional
Decision Date
1999-11-09
Sponsor / Applicant
Wako Chemicals USA, Inc.

Technical Specification

510(k) Submission ID K993466
Product Code CDT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1705
Decision Date 1999-11-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WAKO L-TYPE TRIGLYCERIDE TEST received FDA 510(k) clearance under submission number K993466, sponsored by Wako Chemicals USA, 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 1999-11-09.

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.