meddevicedb.com FDA Device Reference

VISION (TM) HDL CHOLESTEROL

K871461 Class I Traditional
Decision Date
1987-05-14
Sponsor / Applicant
Abbott Laboratories

Technical Specification

510(k) Submission ID K871461
Product Code LBS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1475
Decision Date 1987-05-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VISION (TM) HDL CHOLESTEROL received FDA 510(k) clearance under submission number K871461, sponsored by Abbott Laboratories. 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 1987-05-14.

Classification & Regulation

This clearance is catalogued under FDA product code LBS and 21 CFR 862.1475, within the Clinical Chemistry review panel as a Class I device.