meddevicedb.com FDA Device Reference

FINNIGAN MAT INCOS 50

K873603 Class I Traditional
Decision Date
1987-09-22
Sponsor / Applicant
Finnigan Corp.

Technical Specification

510(k) Submission ID K873603
Product Code JJO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2540
Decision Date 1987-09-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FINNIGAN MAT INCOS 50 received FDA 510(k) clearance under submission number K873603, sponsored by Finnigan 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 1987-09-22.

Classification & Regulation

This clearance is catalogued under FDA product code JJO and 21 CFR 862.2540, within the Clinical Chemistry review panel as a Class I device.