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OPTI LION ELECTROLYTE ANALYZER, MODEL GD7200

K052027 Class II Traditional
Decision Date
2005-09-29
Sponsor / Applicant
Osmetech, Inc.

Technical Specification

510(k) Submission ID K052027
Product Code CGZ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1170
Decision Date 2005-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPTI LION ELECTROLYTE ANALYZER, MODEL GD7200 received FDA 510(k) clearance under submission number K052027, sponsored by Osmetech, 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 2005-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code CGZ and 21 CFR 862.1170, within the Clinical Chemistry review panel as a Class II device.