meddevicedb.com FDA Device Reference

GEM PREMIER PLUS MODEL 5500

K961335 Class II Traditional
Decision Date
1996-06-28
Sponsor / Applicant
Mallinckrodt Sensor Systems, Inc.

Technical Specification

510(k) Submission ID K961335
Product Code CHL
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1120
Decision Date 1996-06-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GEM PREMIER PLUS MODEL 5500 received FDA 510(k) clearance under submission number K961335, sponsored by Mallinckrodt Sensor Systems, 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 1996-06-28.

Classification & Regulation

This clearance is catalogued under FDA product code CHL and 21 CFR 862.1120, within the Clinical Chemistry review panel as a Class II device.