meddevicedb.com FDA Device Reference

METROLAB MODEL 1500

K910806 Class I Traditional
Decision Date
1991-08-30
Sponsor / Applicant
Laboratorio Rodriguez Corswant S.R.L.

Technical Specification

510(k) Submission ID K910806
Product Code JJQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2300
Decision Date 1991-08-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

METROLAB MODEL 1500 received FDA 510(k) clearance under submission number K910806, sponsored by Laboratorio Rodriguez Corswant S.R.L.. 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 1991-08-30.

Classification & Regulation

This clearance is catalogued under FDA product code JJQ and 21 CFR 862.2300, within the Clinical Chemistry review panel as a Class I device.