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BLOOD GAS, ELECTROLYTE AND METABOLITE TEST CARD

K090109 Class II Traditional
Decision Date
2009-06-24
Sponsor / Applicant
Epocal, Inc.

Technical Specification

510(k) Submission ID K090109
Product Code CGA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2009-06-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BLOOD GAS, ELECTROLYTE AND METABOLITE TEST CARD received FDA 510(k) clearance under submission number K090109, sponsored by Epocal, 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 2009-06-24.

Classification & Regulation

This clearance is catalogued under FDA product code CGA and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.