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EML105 ELECTROLYTE METABOLITE ANALYZER

K962334 Class II Traditional
Decision Date
1996-10-24
Sponsor / Applicant
Radiometer America, Inc.

Technical Specification

510(k) Submission ID K962334
Product Code JGS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1665
Decision Date 1996-10-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EML105 ELECTROLYTE METABOLITE ANALYZER received FDA 510(k) clearance under submission number K962334, sponsored by Radiometer America, 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 1996-10-24.

Classification & Regulation

This clearance is catalogued under FDA product code JGS and 21 CFR 862.1665, within the Clinical Chemistry review panel as a Class II device.