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NOVA 10 SODIUM/POTASSIUM/TOTAL CALCIU

K833153 Class I Traditional
Decision Date
1983-11-25
Sponsor / Applicant
Nova Biomedical Corp.

Technical Specification

510(k) Submission ID K833153
Product Code JJF
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2170
Decision Date 1983-11-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NOVA 10 SODIUM/POTASSIUM/TOTAL CALCIU received FDA 510(k) clearance under submission number K833153, 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 1983-11-25.

Classification & Regulation

This clearance is catalogued under FDA product code JJF and 21 CFR 862.2170, within the Clinical Chemistry review panel as a Class I device.