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ANALYZER, SODIUM/POTASSIUM

K791175 Class II Traditional
Decision Date
1979-08-10
Sponsor / Applicant
Nova Biomedical Corp.

Technical Specification

510(k) Submission ID K791175
Product Code CEM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1600
Decision Date 1979-08-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANALYZER, SODIUM/POTASSIUM received FDA 510(k) clearance under submission number K791175, sponsored by Nova Biomedical 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 1979-08-10.

Classification & Regulation

This clearance is catalogued under FDA product code CEM and 21 CFR 862.1600, within the Clinical Chemistry review panel as a Class II device.