meddevicedb.com FDA Device Reference

PERIDOCHROM TRIGLYCERIDES GPO

K850667 Class I Traditional
Decision Date
1985-03-11
Sponsor / Applicant
Boehringer Mannheim Corp.

Technical Specification

510(k) Submission ID K850667
Product Code CDT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1705
Decision Date 1985-03-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PERIDOCHROM TRIGLYCERIDES GPO received FDA 510(k) clearance under submission number K850667, sponsored by Boehringer Mannheim Corp.. 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 1985-03-11.

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.